WO2022107999A1 - Antiviral composition for sars-cov-2 and hcov-oc43 comprising rhein, meclofenamic acid, or a combination thereof - Google Patents
Antiviral composition for sars-cov-2 and hcov-oc43 comprising rhein, meclofenamic acid, or a combination thereof Download PDFInfo
- Publication number
- WO2022107999A1 WO2022107999A1 PCT/KR2021/001312 KR2021001312W WO2022107999A1 WO 2022107999 A1 WO2022107999 A1 WO 2022107999A1 KR 2021001312 W KR2021001312 W KR 2021001312W WO 2022107999 A1 WO2022107999 A1 WO 2022107999A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- cov
- antiviral composition
- coronavirus
- sars
- hcov
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 81
- 230000000840 anti-viral effect Effects 0.000 title claims abstract description 71
- SBDNJUWAMKYJOX-UHFFFAOYSA-N Meclofenamic Acid Chemical compound CC1=CC=C(Cl)C(NC=2C(=CC=CC=2)C(O)=O)=C1Cl SBDNJUWAMKYJOX-UHFFFAOYSA-N 0.000 title claims abstract description 52
- 229960003803 meclofenamic acid Drugs 0.000 title claims abstract description 51
- 241001678559 COVID-19 virus Species 0.000 claims abstract description 46
- 241000008904 Betacoronavirus Species 0.000 claims abstract description 33
- 241001428935 Human coronavirus OC43 Species 0.000 claims abstract description 33
- 208000025721 COVID-19 Diseases 0.000 claims abstract description 23
- 241000700605 Viruses Species 0.000 claims description 28
- 201000003176 Severe Acute Respiratory Syndrome Diseases 0.000 claims description 27
- 239000004480 active ingredient Substances 0.000 claims description 18
- 239000008194 pharmaceutical composition Substances 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 13
- 108090000623 proteins and genes Proteins 0.000 claims description 11
- 241000711573 Coronaviridae Species 0.000 claims description 9
- 102000004169 proteins and genes Human genes 0.000 claims description 9
- 241000315672 SARS coronavirus Species 0.000 claims description 8
- 101710172711 Structural protein Proteins 0.000 claims description 8
- -1 Nsp2 Proteins 0.000 claims description 7
- 239000012528 membrane Substances 0.000 claims description 7
- 241001109669 Human coronavirus HKU1 Species 0.000 claims description 6
- 206010035737 Pneumonia viral Diseases 0.000 claims description 6
- 206010046306 Upper respiratory tract infection Diseases 0.000 claims description 6
- 239000003937 drug carrier Substances 0.000 claims description 6
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 6
- 239000003381 stabilizer Substances 0.000 claims description 6
- 208000009421 viral pneumonia Diseases 0.000 claims description 6
- 241000127282 Middle East respiratory syndrome-related coronavirus Species 0.000 claims description 5
- 101800000935 Non-structural protein 12 Proteins 0.000 claims description 5
- 101800001554 RNA-directed RNA polymerase Proteins 0.000 claims description 5
- 239000003085 diluting agent Substances 0.000 claims description 5
- 201000009240 nasopharyngitis Diseases 0.000 claims description 5
- 230000000241 respiratory effect Effects 0.000 claims description 4
- 101800000515 Non-structural protein 3 Proteins 0.000 claims description 3
- 101800000508 Non-structural protein 5 Proteins 0.000 claims description 3
- 101800000509 Non-structural protein 8 Proteins 0.000 claims description 3
- 101800001728 Nsp1 Proteins 0.000 claims description 3
- 101800001631 3C-like serine proteinase Proteins 0.000 claims description 2
- 108090000371 Esterases Proteins 0.000 claims description 2
- 101800003471 Helicase Proteins 0.000 claims description 2
- 101800000355 Helicase nsp10 Proteins 0.000 claims description 2
- 101800000507 Non-structural protein 6 Proteins 0.000 claims description 2
- 101800000706 Serine protease nsp4 Proteins 0.000 claims description 2
- 101800001925 Uridylate-specific endoribonuclease nsp11 Proteins 0.000 claims description 2
- 108010028403 hemagglutinin esterase Proteins 0.000 claims description 2
- 208000011580 syndromic disease Diseases 0.000 claims description 2
- 108020000999 Viral RNA Proteins 0.000 abstract description 20
- FCDLCPWAQCPTKC-UHFFFAOYSA-N Rhein Chemical compound C1=CC=C2C(=O)C3=CC(C(=O)O)=CC(O)=C3C(=O)C2=C1O FCDLCPWAQCPTKC-UHFFFAOYSA-N 0.000 abstract description 3
- 210000004027 cell Anatomy 0.000 description 81
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 42
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 34
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 24
- 210000003501 vero cell Anatomy 0.000 description 22
- 238000011160 research Methods 0.000 description 20
- 238000011282 treatment Methods 0.000 description 14
- 230000009385 viral infection Effects 0.000 description 14
- 102100031181 Glyceraldehyde-3-phosphate dehydrogenase Human genes 0.000 description 13
- 108020004445 glyceraldehyde-3-phosphate dehydrogenase Proteins 0.000 description 13
- 108091003079 Bovine Serum Albumin Proteins 0.000 description 12
- 239000012091 fetal bovine serum Substances 0.000 description 12
- 239000006144 Dulbecco’s modified Eagle's medium Substances 0.000 description 10
- 238000011529 RT qPCR Methods 0.000 description 10
- 201000010099 disease Diseases 0.000 description 10
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 10
- 239000001963 growth medium Substances 0.000 description 10
- 239000006143 cell culture medium Substances 0.000 description 9
- 230000002401 inhibitory effect Effects 0.000 description 9
- 244000309467 Human Coronavirus Species 0.000 description 8
- 238000002123 RNA extraction Methods 0.000 description 8
- 210000000130 stem cell Anatomy 0.000 description 7
- 238000005516 engineering process Methods 0.000 description 6
- 210000000981 epithelium Anatomy 0.000 description 6
- JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 description 6
- 101710105008 RNA-binding protein Proteins 0.000 description 5
- 208000015181 infectious disease Diseases 0.000 description 5
- 230000002265 prevention Effects 0.000 description 5
- 208000024891 symptom Diseases 0.000 description 5
- 108091034117 Oligonucleotide Proteins 0.000 description 4
- 208000036142 Viral infection Diseases 0.000 description 4
- 230000004069 differentiation Effects 0.000 description 4
- 238000011534 incubation Methods 0.000 description 4
- 239000002609 medium Substances 0.000 description 4
- 239000011259 mixed solution Substances 0.000 description 4
- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 description 4
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 description 4
- 208000023504 respiratory system disease Diseases 0.000 description 4
- 208000010507 Adenocarcinoma of Lung Diseases 0.000 description 3
- 241000282552 Chlorocebus aethiops Species 0.000 description 3
- 206010009944 Colon cancer Diseases 0.000 description 3
- 101800001768 Exoribonuclease Proteins 0.000 description 3
- 241000282412 Homo Species 0.000 description 3
- 101800004575 RNA-directed RNA polymerase nsp12 Proteins 0.000 description 3
- 230000001154 acute effect Effects 0.000 description 3
- 239000002221 antipyretic Substances 0.000 description 3
- 239000003443 antiviral agent Substances 0.000 description 3
- 208000029742 colonic neoplasm Diseases 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 229960000890 hydrocortisone Drugs 0.000 description 3
- 201000005249 lung adenocarcinoma Diseases 0.000 description 3
- 230000001717 pathogenic effect Effects 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 230000001629 suppression Effects 0.000 description 3
- WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 2
- RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 description 2
- 239000005541 ACE inhibitor Substances 0.000 description 2
- 241000004175 Coronavirinae Species 0.000 description 2
- 241000124008 Mammalia Species 0.000 description 2
- 108060004795 Methyltransferase Proteins 0.000 description 2
- 206010035664 Pneumonia Diseases 0.000 description 2
- 102000004005 Prostaglandin-endoperoxide synthases Human genes 0.000 description 2
- 108090000459 Prostaglandin-endoperoxide synthases Proteins 0.000 description 2
- 206010057190 Respiratory tract infections Diseases 0.000 description 2
- 229940044094 angiotensin-converting-enzyme inhibitor Drugs 0.000 description 2
- 230000003110 anti-inflammatory effect Effects 0.000 description 2
- 229940125716 antipyretic agent Drugs 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 230000034303 cell budding Effects 0.000 description 2
- 238000012258 culturing Methods 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 231100000673 dose–response relationship Toxicity 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 238000009511 drug repositioning Methods 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 210000003292 kidney cell Anatomy 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 210000004962 mammalian cell Anatomy 0.000 description 2
- 244000052769 pathogen Species 0.000 description 2
- 230000010076 replication Effects 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 238000013518 transcription Methods 0.000 description 2
- 230000035897 transcription Effects 0.000 description 2
- 230000029812 viral genome replication Effects 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- 102000040650 (ribonucleotides)n+m Human genes 0.000 description 1
- OHVLMTFVQDZYHP-UHFFFAOYSA-N 1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-2-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound N1N=NC=2CN(CCC=21)C(CN1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)=O OHVLMTFVQDZYHP-UHFFFAOYSA-N 0.000 description 1
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 1
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- LDXJRKWFNNFDSA-UHFFFAOYSA-N 2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound C1CN(CC2=NNN=C21)CC(=O)N3CCN(CC3)C4=CN=C(N=C4)NCC5=CC(=CC=C5)OC(F)(F)F LDXJRKWFNNFDSA-UHFFFAOYSA-N 0.000 description 1
- SXAMGRAIZSSWIH-UHFFFAOYSA-N 2-[3-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,2,4-oxadiazol-5-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NOC(=N1)CC(=O)N1CC2=C(CC1)NN=N2 SXAMGRAIZSSWIH-UHFFFAOYSA-N 0.000 description 1
- ZRPAUEVGEGEPFQ-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]pyrazol-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C=NN(C=1)CC(=O)N1CC2=C(CC1)NN=N2 ZRPAUEVGEGEPFQ-UHFFFAOYSA-N 0.000 description 1
- JVKRKMWZYMKVTQ-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]pyrazol-1-yl]-N-(2-oxo-3H-1,3-benzoxazol-6-yl)acetamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C=NN(C=1)CC(=O)NC1=CC2=C(NC(O2)=O)C=C1 JVKRKMWZYMKVTQ-UHFFFAOYSA-N 0.000 description 1
- YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical compound N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 235000006491 Acacia senegal Nutrition 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 241000004176 Alphacoronavirus Species 0.000 description 1
- 101710129690 Angiotensin-converting enzyme inhibitor Proteins 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 101710086378 Bradykinin-potentiating and C-type natriuretic peptides Proteins 0.000 description 1
- 241000282472 Canis lupus familiaris Species 0.000 description 1
- 206010011224 Cough Diseases 0.000 description 1
- 206010050685 Cytokine storm Diseases 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 230000004544 DNA amplification Effects 0.000 description 1
- 241001461743 Deltacoronavirus Species 0.000 description 1
- 206010012735 Diarrhoea Diseases 0.000 description 1
- 208000000059 Dyspnea Diseases 0.000 description 1
- 206010013975 Dyspnoeas Diseases 0.000 description 1
- 201000011001 Ebola Hemorrhagic Fever Diseases 0.000 description 1
- 241000283086 Equidae Species 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- 241000008920 Gammacoronavirus Species 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 206010019233 Headaches Diseases 0.000 description 1
- 208000000616 Hemoptysis Diseases 0.000 description 1
- 102100034343 Integrase Human genes 0.000 description 1
- OFFWOVJBSQMVPI-RMLGOCCBSA-N Kaletra Chemical compound N1([C@@H](C(C)C)C(=O)N[C@H](C[C@H](O)[C@H](CC=2C=CC=CC=2)NC(=O)COC=2C(=CC=CC=2C)C)CC=2C=CC=CC=2)CCCNC1=O.N([C@@H](C(C)C)C(=O)N[C@H](C[C@H](O)[C@H](CC=1C=CC=CC=1)NC(=O)OCC=1SC=NC=1)CC=1C=CC=CC=1)C(=O)N(C)CC1=CSC(C(C)C)=N1 OFFWOVJBSQMVPI-RMLGOCCBSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 1
- 208000025370 Middle East respiratory syndrome Diseases 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- 206010028813 Nausea Diseases 0.000 description 1
- 206010068319 Oropharyngeal pain Diseases 0.000 description 1
- 241000282579 Pan Species 0.000 description 1
- 241000282520 Papio Species 0.000 description 1
- 201000007100 Pharyngitis Diseases 0.000 description 1
- 241000282405 Pongo abelii Species 0.000 description 1
- 206010036790 Productive cough Diseases 0.000 description 1
- 206010037660 Pyrexia Diseases 0.000 description 1
- 230000006819 RNA synthesis Effects 0.000 description 1
- 108010092799 RNA-directed DNA polymerase Proteins 0.000 description 1
- 238000011530 RNeasy Mini Kit Methods 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 208000037847 SARS-CoV-2-infection Diseases 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 241000282887 Suidae Species 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical class NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 1
- 239000003430 antimalarial agent Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 229960001714 calcium phosphate Drugs 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- 229960003340 calcium silicate Drugs 0.000 description 1
- 235000012241 calcium silicate Nutrition 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 238000004113 cell culture Methods 0.000 description 1
- 230000009134 cell regulation Effects 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 206010052015 cytokine release syndrome Diseases 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 238000012377 drug delivery Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000029578 entry into host Effects 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 230000029142 excretion Effects 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 229940014259 gelatin Drugs 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 231100000869 headache Toxicity 0.000 description 1
- XXSMGPRMXLTPCZ-UHFFFAOYSA-N hydroxychloroquine Chemical compound ClC1=CC=C2C(NC(C)CCCN(CCO)CC)=CC=NC2=C1 XXSMGPRMXLTPCZ-UHFFFAOYSA-N 0.000 description 1
- 229960004171 hydroxychloroquine Drugs 0.000 description 1
- 239000003018 immunosuppressive agent Substances 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000010255 intramuscular injection Methods 0.000 description 1
- 239000007927 intramuscular injection Substances 0.000 description 1
- 239000007928 intraperitoneal injection Substances 0.000 description 1
- 238000010253 intravenous injection Methods 0.000 description 1
- 210000001985 kidney epithelial cell Anatomy 0.000 description 1
- 230000002147 killing effect Effects 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229940113983 lopinavir / ritonavir Drugs 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 201000005202 lung cancer Diseases 0.000 description 1
- 208000020816 lung neoplasm Diseases 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 206010025482 malaise Diseases 0.000 description 1
- 238000007726 management method Methods 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229940013798 meclofenamate Drugs 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 1
- 239000008108 microcrystalline cellulose Substances 0.000 description 1
- 229940016286 microcrystalline cellulose Drugs 0.000 description 1
- 230000003278 mimic effect Effects 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 230000008693 nausea Effects 0.000 description 1
- 239000002547 new drug Substances 0.000 description 1
- 108020004707 nucleic acids Proteins 0.000 description 1
- 102000039446 nucleic acids Human genes 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 201000008482 osteoarthritis Diseases 0.000 description 1
- 229940094443 oxytocics prostaglandins Drugs 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- 150000003180 prostaglandins Chemical class 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000002797 proteolythic effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000003753 real-time PCR Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- RWWYLEGWBNMMLJ-MEUHYHILSA-N remdesivir Drugs C([C@@H]1[C@H]([C@@H](O)[C@@](C#N)(O1)C=1N2N=CN=C(N)C2=CC=1)O)OP(=O)(N[C@@H](C)C(=O)OCC(CC)CC)OC1=CC=CC=C1 RWWYLEGWBNMMLJ-MEUHYHILSA-N 0.000 description 1
- RWWYLEGWBNMMLJ-YSOARWBDSA-N remdesivir Chemical compound NC1=NC=NN2C1=CC=C2[C@]1([C@@H]([C@@H]([C@H](O1)CO[P@](=O)(OC1=CC=CC=C1)N[C@H](C(=O)OCC(CC)CC)C)O)O)C#N RWWYLEGWBNMMLJ-YSOARWBDSA-N 0.000 description 1
- 210000002345 respiratory system Anatomy 0.000 description 1
- 230000001624 sedative effect Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000010356 sorbitol Nutrition 0.000 description 1
- 208000024794 sputum Diseases 0.000 description 1
- 210000003802 sputum Anatomy 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000010254 subcutaneous injection Methods 0.000 description 1
- 239000007929 subcutaneous injection Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 230000009469 supplementation Effects 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 238000002636 symptomatic treatment Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 229960003989 tocilizumab Drugs 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229960005486 vaccine Drugs 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 230000006656 viral protein synthesis Effects 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/196—Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
Definitions
- the present invention was made under the project specific number 1711101405 under the support of the Ministry of Science and ICT of the Republic of Korea.
- the research management institution for the project is the Seoul National University Industry-Academic Cooperation Foundation, and the research project name is "Creation of an International Science Business Belt (Research Operational Support for Basic Science Research Institute) ", the research project title is "Study on the regulation of cell fate by RNA", the lead institution is the Institute for Basic Science, and the research period is 2020.03.03.-2020.08.28.
- the present invention provides anti-SARS-CoV-2 and HCoV- OC43 of the genus betacoronavirus comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient It relates to a composition for viruses.
- Coronavirus is an enveloped virus with a positive-sense single-stranded RNA genome and belongs to the family Coronavirinae .
- coronavirus family is divided into four genera: alpha, beta, gamma and delta coronaviruses. Seven types of coronaviruses that infect humans have been discovered so far, and five of them belong to betacoronaviruses.
- Severe Acute Respiratory Syndrome Coronavirus 2 which started to cause pneumonia of unknown cause in Wuhan, China in December 2019 and caused coronavirus disease 19 (COVID-19), an acute respiratory disease epidemic worldwide (severe acute respiratory syndrome coronavirus 2, SARS-CoV-2) is also classified as a beta-coronavirus.
- remdesivir an antiviral drug developed to treat Ebola, hydroxychloroquine, an antimalarial drug, lopinavir/ritonavir, an HIV drug, and an immunosuppressant drug that suppresses cytokine storm Tocilizumab and angiotensin-converting enzyme inhibitor (ACE inhibitor) are being administered for emergency use to COVID-19 patients or are in clinical trials.
- ACE inhibitor angiotensin-converting enzyme inhibitor
- rhein is an anthraquinone derivative and has an anti-inflammatory effect, so it has been used for the treatment of degenerative arthritis. It is used as a non-steroidal anti-inflammatory drug (NSAID) and as an antipyretic agent.
- NSAID non-steroidal anti-inflammatory drug
- the antiviral effect of the two compounds against SARS-CoV-2 and HCoV-OC43 belonging to betacoronaviruses is unknown.
- the present inventors made intensive research efforts to develop an antiviral composition for beta coronavirus . As a result, it was found that a composition comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient significantly inhibits viral RNA, thereby completing the present invention.
- an object of the present invention to provide an antiviral composition for beta-coronavirus comprising rhein , meclofenamic acid, or a combination thereof as an active ingredient.
- Another object of the present invention is to provide an antiviral composition for SARS-CoV-2 and HCoV-OC43 comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient.
- Another object of the present invention is to provide a pharmaceutical composition for preventing or treating COVID-19 (Coronavirus Disease 2019).
- Another object of the present invention is a pharmaceutical composition for the prevention or treatment of common cold, acute upper respiratory tract infection, severe acute respiratory syndrome or viral pneumonia is to provide
- the present invention provides an antiviral composition for beta coronavirus comprising rhein , meclofenamic acid, or a combination thereof as an active ingredient. .
- the present inventors made intensive research efforts to develop an antiviral composition for beta coronavirus . As a result, it was found that a composition comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient significantly inhibits viral RNA.
- Rhein of the present invention is an anthraquinone derivative, also known as cassic acid and 4,5-dihydroxy-9,10-dioxoanthracene-2-carboxylic acid, and has an anti-inflammatory effect. It refers to a compound represented by the following formula (1), which is being used.
- meclofenamic acid of the present invention is an anthranilic acid derivative, also known as meclofenamate, a cyclooxygenase (COX) inhibitor, and has the effect of inhibiting the formation of prostaglandins. It refers to a compound represented by the following Chemical Formula 2, which is used as a non-steroidal anti-inflammatory drug (NSAID) and an antipyretic agent.
- NSAID non-steroidal anti-inflammatory drug
- the term “comprising as an active ingredient” means including an amount sufficient to achieve pharmacological efficacy or activity of rhein, meclofenamic acid, or a combination thereof, It means that various components may be additionally added for drug delivery, stabilization and formulation.
- antiviral composition refers to virus invasion into host cells, viral genome replication and synthesis, viral genome transcription, viral protein synthesis, reverse transcriptase activity, virus assembly or virus budding (budding). ) by inhibiting a composition for preventing infection of the virus, inhibiting the replication of the virus, preventing the spread of the virus, or killing the virus, or a composition for treating a disease caused by virus infection or symptoms expressed by it it means.
- prevention refers to the prevention or protective treatment of a disease or disease state.
- treatment means reducing, suppressing, sedating, or eradicating a disease state.
- betacoronavirus ' is one of four genus belonging to the family Coronavirinae , and RNA that infects animals and humans and causes asymptomatic or mild to severe respiratory symptoms means virus.
- the beta coronavirus of the present invention is HCoV-OC43 (human coronavirus OC43 ), HCoV-HKU1 (human coronavirus HKU1), SARS-CoV (severe acute respiratory syndrome coronavirus), MERS- Middle East respiratory syndrome coronavirus (CoV) and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
- beta coronavirus of the present invention includes SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) and HCoV-OC43 (human coronavirus OC43 ).
- the active ingredient of the present invention is the non-structural protein (Nsp), spike (S), envelope (E), membrane (membrane, M) of the beta coronavirus. ), nucleocapsid (nucleocapsid, N) and hemagglutinin esterase (haemagglutinin esterase, HE) characterized in that it inhibits the level of at least one viral RNA selected from the group consisting of proteins.
- the active ingredient of the present invention is a non-structural protein (Nsp), a membrane (M) protein, and a nucleocapsid (N) protein of the beta coronavirus. It is characterized in that it inhibits the level of at least one or more viral RNAs selected from the group consisting of.
- non-structural protein refers to a non-structural protein related to the replication and transcription of coronavirus.
- Non-structural proteins of coronavirus include 16 Nsp1 to Nsp16, Nsp3 and Nsp5 have proteolytic activity, and Nsp7, Nsp8 and Nsp12 form a replicase-transcriptase complex (RTC).
- RTC replicase-transcriptase complex
- Nsp12 a key component of RTC, is an RNA-dependent RNA polymerase (RdRp) and directly mediates RNA synthesis in viral replication.
- the non-structural protein (Nsp) of the present invention is Nsp1, Nsp2, Nsp3, Nsp4, Nsp5, Nsp6, Nsp7, Nsp8, Nsp9, Nsp10, Nsp11, Nsp12, Nsp13, Nsp14 , at least one protein selected from the group consisting of Nsp15 and Nsp16.
- the nonstructural protein of the present invention is Nsp12.
- the antiviral composition of the present invention additionally comprises a pharmaceutically acceptable carrier, carrier, excipient, stabilizer or diluent.
- the pharmaceutically acceptable carrier, carrier, excipient, stabilizer or diluent of the present invention is commonly used in the art to which the present invention pertains and is pharmaceutically compatible with the active ingredient of the present invention. means
- Pharmaceutically acceptable carriers or carriers of the pharmaceutical composition of the present invention include lactose, dextrose, sucrose, sorbitol, mannitol, starch, gum acacia, calcium phosphate, alginate, gelatin, calcium silicate, microcrystalline cellulose, poly vinylpyrrolidone, cellulose, water, syrup, methyl cellulose, methylhydroxybenzoate, propylhydroxybenzoate, talc, magnesium stearate, mineral oil, ethanol, dimethyl sulfoxide (DMSO), etc.
- DMSO dimethyl sulfoxide
- the pharmaceutical composition of the present invention may further include excipients, stabilizers, diluents, lubricants, wetting agents, sweeteners, flavoring agents, emulsifiers, suspending agents, preservatives, and the like, in addition to the above components.
- excipients stabilizers, diluents, lubricants, wetting agents, sweeteners, flavoring agents, emulsifiers, suspending agents, preservatives, and the like.
- Suitable pharmaceutically acceptable carriers, carriers, excipients, stabilizers or diluents are described in detail in Remington's Pharmaceutical Sciences (19th ed., 1995).
- the pharmaceutical composition of the present invention may be administered orally or parenterally, and in the case of parenteral administration, it may be administered by intravenous injection, subcutaneous injection, intramuscular injection, intraperitoneal injection, transdermal administration, or the like.
- a suitable dosage of the pharmaceutical composition of the present invention varies depending on factors such as formulation method, administration method, age, weight, sex, pathological condition, food, administration time, administration route, excretion rate and response sensitivity of the patient, An ordinarily skilled physician can readily determine and prescribe a dosage effective for the desired treatment or prophylaxis. Meanwhile, the dosage of the pharmaceutical composition of the present invention is preferably 0.0001-1000 mg/kg (body weight) per day.
- the pharmaceutical composition of the present invention is prepared in unit dosage form by formulating using a pharmaceutically acceptable carrier and/or excipient according to a method that can be easily performed by a person of ordinary skill in the art to which the present invention pertains. or it may be prepared by incorporation into a multi-dose container.
- the formulation may be in the form of a solution, suspension, or emulsion in oil or aqueous medium, or may be in the form of an extract, powder, granule, tablet or capsule, and may additionally include a dispersant or stabilizer.
- the mammalian cells used in the present invention include Vero cell line (African green monkey kidney cell line), Calu-3 cell line (human lung adenocarcinoma cell line), HBEC cell line (human bronchial epithelium cell line), and HCT-8 cell line (colon cancer). cell line), including at least one or more mammalian cells selected from the group consisting of, but not limited thereto.
- the Vero cell line of the present invention is a cell line isolated from kidney epithelial cells of an African green monkey, and is often used as a host cell for virus culture.
- the Calu-3 cell line of the present invention is a cell line derived from human lung cancer cells (human lung adenocarcinoma cell line), which is commonly used in research on respiratory infection viruses and is used in SARS-CoV-2 research.
- the HBEC cell line of the present invention is a human bronchial epithelium cell line, and a cell culture medium - bronchial epithelium cells differentiated from stem cells - is a cell line cultured in the air layer to mimic the actual respiratory system one step further in cell culture research.
- the HCT-8 cell of the present invention is a colon cancer cell line, a cell line commonly used in HCoV-OC43 research.
- the present invention provides a pharmaceutical composition for preventing or treating COVID-19 (coronavirus disease 2019) comprising the above-described antiviral composition.
- COVID-19 is a respiratory disease caused by SARS-CoV-2 infection, meaning coronavirus disease 2019 (COVID-19), and is asymptomatic or has fever, malaise, cough, dyspnea, It shows mild to severe respiratory symptoms including pneumonia, sputum, sore throat, headache, hemoptysis, nausea, and diarrhea.
- COVID-19 is a respiratory disease caused by SARS-CoV-2 infection, meaning coronavirus disease 2019 (COVID-19), and is asymptomatic or has fever, malaise, cough, dyspnea, It shows mild to severe respiratory symptoms including pneumonia, sputum, sore throat, headache, hemoptysis, nausea, and diarrhea.
- there are conservative treatments such as fluid supplementation and/or the use of antipyretic drugs, and there is no antiviral agent for SARS-CoV-2.
- the pharmaceutical composition for the prevention or treatment of COVID-19 (coronavirus disease 2019) of the present invention includes the antiviral composition of another aspect of the present invention described above, overlapping contents are included in order to avoid excessive complexity of the present specification. cited, and the description thereof is omitted.
- the present invention provides a common cold, acute upper respiratory tract infection, severe acute respiratory syndrome or virus comprising the above-described antiviral composition. It provides a pharmaceutical composition for preventing or treating viral pneumonia.
- the pharmaceutical composition for preventing or treating common cold, acute upper respiratory tract infection, severe acute respiratory syndrome, or viral pneumonia of the present invention is the present invention Since it includes the antiviral composition of another aspect of the present invention, overlapping content is cited in order to avoid excessive complexity of the description of the present specification, and the description thereof is omitted.
- the present invention is a beta coronavirus comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient according to another aspect of the present invention described above.
- Betacoronavirus provides a virus suppression method comprising administering an antiviral composition to a subject in need thereof.
- the present invention is a beta coronavirus comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient according to another aspect of the present invention described above.
- Betacoronavirus provides a method of treating a disease caused by a viral infection comprising administering an antiviral composition to a subject in need thereof.
- Viruses and diseases subject to the virus suppression method and disease treatment method of the present invention are the same as those defined in the antiviral composition described above.
- the subject of the present invention is a mammal or a human.
- the mammal includes, but is not limited to, dogs, cats, cows, horses, pigs, mice, rats, chimpanzees, orangutans, baboons, and the like.
- the present invention provides an antiviral composition for beta coronavirus comprising rhein , meclofenamic acid, or a combination thereof as an active ingredient.
- the present invention provides an antiviral composition for SARS-CoV-2 and HCoV-OC43 comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient.
- the present invention is administered to a subject in need of an antiviral composition for beta coronavirus comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient It provides a virus suppression method comprising the step of.
- the present invention is administered to a subject in need of a composition for antiviral against beta-coronavirus comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient It provides a method for treating diseases caused by viral infection comprising the step of:
- RNA level of beta-coronavirus when using the antiviral composition of the present invention, by suppressing the RNA level of beta-coronavirus, COVID-19 (coronavirus disease 2019), common cold, acute upper respiratory tract infection (acute upper respiratory tract infection), severe It can prevent or treat severe acute respiratory syndrome or viral pneumonia.
- FIG. 1A to 1D show the viral RNA levels measured by qRT-PCR according to whether or not SARS-CoV-2 or HCoV-OC43-infected cells are treated with an antiviral composition including rhein.
- Figure 1a shows Calu-3 cells infected with SARS-CoV-2 (SARS-CoV-2-infected Calu-3)
- Figure 1b shows Vero cells infected with SARS-CoV-2 (SARS-CoV-2-infected Vero)
- 1C shows viral RNA levels in HCoV-OC43 infected HCT-8 cells (HCoV OC43-infected HCT-8)
- FIG. 1D shows viral RNA levels in HCoV-OC43 infected Vero cells (HCoV OC43-infected Vero). All RNA levels were corrected for the RNA level of each GAPDH.
- FIG. 2a to 2e show the viral RNA levels measured by qRT-PCR according to whether or not the SARS-CoV-2 or HCoV-OC43-infected cells were treated with an antiviral composition containing meclofenamic acid (MA). indicates.
- Figure 2a shows Calu-3 cells infected with SARS-CoV-2 (SARS-CoV-2-infected Calu-3)
- Figure 2b shows HBEC cells infected with SARS-CoV-2 (SARS-CoV-2-infected HBEC);
- Fig. 2c shows Vero cells infected with SARS-CoV-2 (SARS-CoV-2-infected Vero), Fig.
- RNA levels in OC43-infected Vero cells are shown. All RNA levels were corrected for the RNA level of each GAPDH.
- Example 1-1 Preparation of antiviral composition comprising Rhein
- Rhein was purchased from Sigma-Aldrich (Catalog No. R7269) to prepare an antiviral composition comprising rhein at concentrations of 5 ⁇ M, 10 ⁇ M, 25 ⁇ M and 50 ⁇ M in vehicle DMSO, DMSO as a control.
- a composition containing only or a mixed solution of 50% (v/v) DMSO and 50% (v/v) ethanol (DMSO + Ethanol) was prepared.
- Example 1-2 Preparation of antiviral composition containing meclofenamic acid (MA)
- Meclofenamic acid (MA) was purchased from Sigma-Aldrich (Cat. No. M4531) and prepared in carrier ethanol at concentrations of 0.5 ⁇ M, 5 ⁇ M, 10 ⁇ M, 25 ⁇ M, 50 ⁇ M and 100 ⁇ M meclofenamic acid (MA). ) was prepared, and as a control, a composition containing only ethanol or a mixed solution of 50% (v/v) DMSO and 50% (v/v) ethanol (DMSO + Ethanol) was prepared.
- Example 2-1 Vero cell line
- Vero cell line African green monkey kidney cell line, ATCC (American Type Culture Collection), catalog number: CCL-81
- DMEM Denssion Medium
- FBS fetal bovine serum
- Calu-3 cell line human lung adenocarcinoma cell line, Korean Cell Line Bank (KCLB), KCLB No.: 30055
- KCLB Korean Cell Line Bank
- the HCT-8 cell line (colon cancer cell line, Korea Cell Line Bank, KCLB No.: 10244) was cultured in an RPMI (Rosewell Park Memorial Institute) culture medium supplemented with 10% FBS at 37° C. and 5% CO 2 in an incubator.
- RPMI Rosewell Park Memorial Institute
- Example 2-4 HBEC cell line
- the HBEC cell line (human bronchial epithelium cell line, ATCC, catalog number: PCS-300-010) was cultured by slightly modifying the protocol provided by STEMCELL TM Technologies ( mutatis mutandis ).
- hydrocortisone hydrocortisone, Sigma, catalog #H0888
- PneumaCult TM -Ex plus medium STMCELL TM Technologies, catalog #05040
- HBEC cells cultured for the above 3 days were placed in a 12-well plate (0.4 ⁇ m between the Basal Chamber below and the Apical Chamber above) at 3 ⁇ 10 5 cells/well.
- HBEC cells formed a pseudostratified epithelium that is morphologically and functionally similar to human airway epithelium in vivo.
- the culture medium PneumaCult TM -ALI maintenance medium (STEMCELL TM Technologies, catalog #05002, 05003 and 05006, 1 ⁇ g/ml of hydrocortisone is added) in a 12-well plate Basal Chamber 2
- the culture medium was changed once a day.
- the culture medium was replaced with the culture medium twice a week for 7 days, and the culture medium was changed once a week for the next 7 days.
- iii) On day 45 after culture, iii) the differentiated and maintained HBEC cells were infected with beta-coronavirus, and iV) samples were obtained for RNA extraction on day 47 after culture, that is, 48 hours after virus infection.
- SARS-CoV-2 severe acute respiratory syndrome coronavirus 2
- SARS-CoV-2 severe acute respiratory syndrome coronavirus 2
- SARS-CoV-2 is a pathogen resource purchased from the National Pathogen Resource Bank under the Korea Centers for Disease Control and Prevention, and was managed under strict control at the International Vaccine Research Institute's biosafety level 3 research facility. .
- HCoV OC43 human coronavirus OC43 was purchased from the Pathogenic Virus Bank of Korea University and managed at a biosafety level 2 research facility.
- Example 4-1 Treatment of an antiviral composition comprising Rhein in a cell line infected with SARS-CoV-2 or HCoV-OC43
- the Calu-3 cell line was cultured in three wells of 1.75 ⁇ 10 5 cells/well in a 12-well plate. After 18 hours of incubation, each well was washed with serum-free DMEM and each well was infected with SARS-CoV-2 at a multiplicity of infection (MOI) of 0.05 in a biosafety grade 3 research facility, 2% Cultured in DMEM containing FBS. Simultaneously with virus infection, an antiviral composition containing 25 ⁇ M concentration of Rhein and DMSO as a control were treated in the cell culture medium of each well. Samples for RNA extraction were obtained 24 hours after viral infection.
- MOI multiplicity of infection
- the Vero cell line was cultured in three wells of 1.75 ⁇ 10 5 cells/well in a 12-well plate. After 18 hours of incubation, each well was washed with serum-free DMEM and infected with SARS-CoV-2 at an MOI of 0.05 in a biosafety grade 3 research facility, and cultured in DMEM containing 2% FBS. Simultaneously with virus infection, an antiviral composition containing 25 ⁇ M concentration of Rhein and DMSO as a control were treated in the cell culture medium of each well. Samples for RNA extraction were obtained 24 hours after viral infection.
- the HCT-8 cell line was cultured in two wells of 2 ⁇ 10 5 cells/well in a 12-well plate. After washing each well with RPMI containing PBS or 3% FBS 18 hours after incubation, HCoV-OC43 was infected in a biosafety grade 2 research facility, and cultured in RPMI containing 3% FBS. Simultaneously with virus infection, a mixed solution of DMSO and ethanol as a control and an antiviral composition containing Rhein at 0.25 ⁇ M, 2.5 ⁇ M, 25 ⁇ M and 250 ⁇ M concentrations was treated in the cell culture medium of each well. 24 hours after virus infection, each well was washed with PBS or RPMI containing 3% FBS to obtain a sample for RNA extraction.
- the Vero cell line was cultured in three wells of 2 ⁇ 10 5 cells/well in a 12-well plate. After 18 hours of incubation, each well was washed with DMEM containing PBS or 3% FBS, and then infected with HCoV-OC43 in a biosafety grade 2 research facility, and cultured in DMEM containing 3% FBS. Simultaneously with virus infection, an antiviral composition containing 5 ⁇ M, 10 ⁇ M, 25 ⁇ M and 50 ⁇ M concentration of Rhein and DMSO as a control were treated in the cell culture medium of each well. 24 hours after virus infection, samples for RNA extraction were obtained after washing with PBS or DMEM containing 3% FBS.
- Example 4-2 Treatment of an antiviral composition containing meclofenamic acid (MA) in a cell line infected with SARS-CoV-2 or HCoV-OC43
- MA meclofenamic acid
- each cell line was cultured under the same or similar conditions as those described in Example 4-1, except for the type of the treated antiviral composition and the HBEC cells infected with SARS-CoV-2, each virus was infected. In order to avoid excessive complexity of the description of the specification, overlapping content is cited and description thereof is omitted.
- SARS-CoV-2-infected Calu-3 cells SARS-CoV-2-infected Calu-3
- SARS-CoV-2 infected HBEC cells SARS-CoV-2-infected HBEC
- SARS-CoV-2 Infected Vero cells SARS-CoV-2-infected Vero
- MA meclofenamic acid
- SARS-CoV-2 infected HBEC cells SARS-CoV-2-infected HBEC cells
- Example 2-4 the cultured HBEC cell line was differentiated and maintained on the 3rd day after culturing, and on the 45th day after culturing, each well was washed with PBS in a biosafety grade 3 research facility, and then SARS-CoV-2 was 3.3 Infected with ⁇ 10 4 pfu (plaque-forming unit).
- SARS-CoV-2 was 3.3 Infected with ⁇ 10 4 pfu (plaque-forming unit).
- an antiviral composition containing 50 ⁇ M of meclofenamic acid (MA) and ethanol as a control were treated in the cell culture medium of each well.
- MA meclofenamic acid
- samples for RNA extraction were obtained.
- RNA extraction obtained in Example 4 was treated with a nucleic acid extraction solution Trizol (Invitrogen, catalog number 10296028) to isolate total RNA.
- Total RNA from cells infected with SARS-CoV-2 was obtained using the PureLink TM RNA Mini Kit (Invitrogen, catalog number: 12183018A), and total RNA from cells infected with HCoV-OC43 was obtained using the RNeasy Mini Kit (Qiagen, catalog number: 74106). and purified according to the manufacturer's protocol. The concentration of purified RNA was measured using a spectrophotometer (NanoDrop TM 2000c Spectrophotometer, ND-2000C, Thermo Scientific).
- the purified RNA obtained in Example 5 was qRT with Power SYBR TM Green PCR Master Mix (Applied Biosystems TM , catalog number: 4367659) and real-time gene amplification equipment (Real-time QuantStudio 3 Real-Time PCR Instrument, Applied Biosystems TM ). -PCR was performed.
- the sequences of the forward (forward, F) and reverse (reverse, R) of the primers used in the qRT-PCR experiment are presented in Table 1 below.
- NSP12 non-structural protein 12
- M membrane
- N nucleocapsid
- primers having the oligonucleotide sequences shown in SEQ ID NOs: 1 to 6 were used.
- SEQ ID NOs: 7 and 8 were used.
- RNA of GAPDH in Vero and HCT-8 cells infected with SARS-CoV-2 primers having the oligonucleotide sequences shown in SEQ ID NOs: 9 and 10 were used.
- primers having the oligonucleotide sequences shown in SEQ ID NOs: 11 and 12 were used.
- Ct (Cycle threshold) values of nsp12 (non-structural protein 12), membrane (M) protein and nucleocapsid (N) protein genes obtained as a result of qRT-PCR experiments were used as Ct values of GAPDH, an endogenous control.
- Virus RNA levels were analyzed using the method of 2 - ⁇ Ct with normalized.
- the experiment of the present invention was repeated at least three times except for the HCT-8 cell infection infected with HCoV-OC43, which was repeated twice, and the error bar on the graph of FIGS. 1A to 1D and 2A to 2E is the standard error of the mean.
- Example 7 Inhibitory effect of beta-coronavirus RNA of antiviral composition comprising Rhein
- Example 7-1 Virus RNA inhibitory effect of antiviral composition containing Rhein on SARS-CoV-2
- nsp12, M measured by qRT-PCR in the control group treated with SARS-CoV-2-infected Calu-3 cells and Vero cells only with DMSO and the experimental group treated with the antiviral composition containing 25 ⁇ M lane (Rhein) And virus RNA levels of N were analyzed by correcting them with GAPDH (see FIGS. 1A and 1B ).
- SARS-CoV-2 SARS-CoV-2-infected Calu-3
- the experimental group treated with an antiviral composition containing 25 ⁇ M of Rhein were all significantly suppressed by less than 5% (see Fig.
- Example 7-2 Virus RNA inhibitory effect of antiviral composition containing Rhein on HCoV-OC43
- HCoV-OC43-infected HCT-8 cells (HCoV OC43-infected HCT-8) were treated with a mixture of DMSO and ethanol (DMSO+Ethanol) in the control group and lanes (Rhein) of 0.25 ⁇ M, 2.5 ⁇ M, 25 ⁇ M and 250 ⁇ M ) in the experimental group treated with an antiviral composition containing
- DMSO+Ethanol DMSO+Ethanol
- lanes Rhein
- the viral RNA level of each N measured by qRT-PCR was analyzed by correcting it with GAPDH.
- Example 8 Inhibitory effect of antiviral composition containing meclofenamic acid (MA) on viral RNA
- Example 8-1 Virus RNA inhibitory effect of antiviral composition containing meclofenamic acid (MA) on SARS-CoV-2
- Calu-3 cells infected with SARS-CoV-2 SARS-CoV-2-infected Calu-3
- HBEC cells SARS-CoV-2-infected HBEC
- Vero cells SARS-CoV-2-infected Vero
- MA meclofenamic acid
- M and N were all significantly suppressed by less than 5% (see FIGS. 2a and 2c ), and in the case of SARS-CoV-2-infected HBEC cells (SARS-CoV-2-infected HBEC), It was significantly suppressed by about 40% or less (see Fig. 2b).
- Example 8-2 Virus RNA inhibitory effect of antiviral composition containing meclofenamic acid (MA) on HCoV-OC43
- HCoV OC43-infected HCT-8 cells HCoV OC43-infected HCT-8 cells
- MA meclofenamic acid
- the viral RNA level of N measured by qRT-PCR was analyzed by correcting it with GAPDH.
- HCT-8 cells infected with HCoV-OC43 were treated with an antiviral composition containing 50 ⁇ M MA
- Vero cells infected with HCoV-OC43 were treated with 10 ⁇ M, 25 ⁇ M, 50 ⁇ M and 100 ⁇ M of MA. It was confirmed that the viral RNA level of N was significantly suppressed when the composition for antiviral containing was treated.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Virology (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
The present invention relates to an antiviral composition for Betacoronavirus comprising rhein and meclofenamic acid as active components. When the antiviral composition of the present invention is used, an antiviral effect is demonstrated whereby the viral RNA level of SARS-CoV-2 and HCoV-OC43 is suppressed, and thus it is possible to treat or prevent COVID-19 or a cold.
Description
본 발명은 대한민국 과학기술정보통신부의 지원 하에서 과제고유번호 1711101405에 의해 이루어진 것으로서, 상기 과제의 연구관리전문기관은 서울대학교 산학협력단, 연구사업명은 "국제과학비즈니스벨트조성(기초과학연구원연구운영비지원)", 연구과제명은 "RNA에 의한 세포 운명 조절 연구”, 주관기관은 기초과학연구원, 연구기간은 2020.03.03.-2020.08.28. 이다.The present invention was made under the project specific number 1711101405 under the support of the Ministry of Science and ICT of the Republic of Korea. The research management institution for the project is the Seoul National University Industry-Academic Cooperation Foundation, and the research project name is "Creation of an International Science Business Belt (Research Operational Support for Basic Science Research Institute) ", the research project title is "Study on the regulation of cell fate by RNA", the lead institution is the Institute for Basic Science, and the research period is 2020.03.03.-2020.08.28.
본 특허출원은 2020년 11월 17일에 대한민국 특허청에 제출된 대한민국 특허출원 제10-2020-0154110호에 대하여 우선권을 주장하며, 상기 특허출원의 개시사항은 본원에 참조로서 삽입된다.This patent application claims priority to Korean Patent Application No. 10-2020-0154110 filed with the Korean Intellectual Property Office on November 17, 2020, the disclosure of which is incorporated herein by reference.
본 발명은 레인(rhein), 메클로페남산(meclofenamic acid), 또는 이들의 조합을 유효성분으로 포함하는 베타코로나바이러스(Betacoronavirus) 속(genus)의 SARS-CoV-2 및 HCoV-OC43에 대한 항바이러스용 조성물에 관한 것이다.The present invention provides anti-SARS-CoV-2 and HCoV- OC43 of the genus betacoronavirus comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient It relates to a composition for viruses.
코로나바이러스(coronavirus, CoV)는 양성-센스 단일 가닥 RNA 유전체를 가진 외피 바이러스(enveloped virus)이며, 코로나바이러스 과(family Coronavirinae)에 속한다. Coronavirus (CoV) is an enveloped virus with a positive-sense single-stranded RNA genome and belongs to the family Coronavirinae .
코로나바이러스 과는 알파, 베타, 감마 및 델타 코로나바이러스의 네 개의 속(genus)으로 분류된다. 사람에게 감염을 일으키는 코로나바이러스는 현재까지 7종이 발견되었고, 이 중 5종이 베타코로나바이러스(betacoronavirus)에 속한다. 가벼운 호흡기 증상을 유발하는 인간 코로나바이러스 OC43(human coronavirus OC43, HCoV-OC43) 및 인간 코로나바이러스 HKU1(human coronavirus HKU1, HCoV-HKU1)와, 치명적인 호흡기 감염을 일으키는 중증급성호흡기증후군 코로나바이러스(severe acute respiratory syndrome coronavirus, SARS-CoV, 사스 코로나바이러스) 및 중동호흡기증후군 코로나바이러스(Middle East respiratory syndrome coronavirus, MERS-CoV, 메르스 코로나바이러스)가 베타코로나바이러스에 속한다.The coronavirus family is divided into four genera: alpha, beta, gamma and delta coronaviruses. Seven types of coronaviruses that infect humans have been discovered so far, and five of them belong to betacoronaviruses. Human coronavirus OC43 (HCoV-OC43) and human coronavirus HKU1 (HCoV-HKU1), which cause mild respiratory symptoms, and severe acute respiratory syndrome coronavirus, which cause fatal respiratory infections Syndrome coronavirus, SARS-CoV, SARS coronavirus) and Middle East respiratory syndrome coronavirus (MERS-CoV, MERS coronavirus) belong to beta-coronaviruses.
특히 2019년 12월에 중국 우한에서 원인 불명의 폐렴을 유발하기 시작하여 전세계적으로 대유행하는 급성 호흡기 질환인 코로나바이러스감염병-19(coronavirus disease 19, COVID-19)를 일으키는 중증급성호흡기증후군 코로나바이러스 2(severe acute respiratory syndrome coronavirus 2, SARS-CoV-2)도 베타코로나바이러스로 분류된다.In particular, Severe Acute Respiratory Syndrome Coronavirus 2, which started to cause pneumonia of unknown cause in Wuhan, China in December 2019 and caused coronavirus disease 19 (COVID-19), an acute respiratory disease epidemic worldwide (severe acute respiratory syndrome coronavirus 2, SARS-CoV-2) is also classified as a beta-coronavirus.
SARS-CoV-2의 감염에 의한 급성 호흡기 질환인 COVID-19에 대한 신규 치료제의 개발이 활발히 연구되고 있고, 신약 개발에 걸리는 시간을 단축하고 비용을 절감하기 위해 기존에 개발된 약물에서 COVID-19의 예방 및 치료 효과를 찾는 약물재창출(drug repurposing 또는 drug repositioning) 전략이 실행되고 있다.The development of new therapeutic agents for COVID-19, an acute respiratory disease caused by infection with SARS-CoV-2, is being actively studied, and in order to shorten the time taken to develop new drugs and reduce costs, COVID-19 from previously developed drugs A drug repurposing or drug repositioning strategy is being implemented to find the preventive and therapeutic effects of
예를 들어, 에볼라 치료제로 개발되었던 항바이러스제 렘데시비르(remdesivir), 말라리아 치료제 하이드록시클로로퀸(hydroxychloroquine), HIV 치료제 로피나비르/리토나비르(lopinavir/ritonavir), 사이토카인 폭풍을 억제하는 면역억제제 토실리주맙(tocilizumab), ACE 억제제(angiotensin-converting enzyme inhibitor) 등이 COVID-19 환자에게 긴급 사용으로 투여되고 있거나 임상시험 중에 있다. 이러한 잠재적 치료제는 COVID-19의 증상을 완화하거나 회복 기간을 단축할 수 있으나, 현재까지 FDA의 승인을 받은 COVID-19 치료제는 없다.For example, remdesivir, an antiviral drug developed to treat Ebola, hydroxychloroquine, an antimalarial drug, lopinavir/ritonavir, an HIV drug, and an immunosuppressant drug that suppresses cytokine storm Tocilizumab and angiotensin-converting enzyme inhibitor (ACE inhibitor) are being administered for emergency use to COVID-19 patients or are in clinical trials. These potential treatments may relieve symptoms of COVID-19 or shorten the recovery period, but to date there is no FDA-approved treatment for COVID-19.
따라서 사람에게 유행성 감염을 일으켜 가벼운 감기부터 치명적인 중증 급성 호흡기 질환까지 유발하는 베타코로나바이러스에 대한 항바이러스제의 개발이 시급한 상황이다.Therefore, there is an urgent need to develop an antiviral agent for beta-coronavirus, which causes epidemics in humans and causes from mild colds to fatal severe acute respiratory diseases.
한편, 레인(rhein)은 안트라퀴논(anthraquinone) 유도체로서 항염증 효과가 있어 기존에 퇴행성관절염의 치료에 사용되고 있고, 메클로페남산(meclofenamic acid)은 안트라닐산(anthranilic acid) 유도체로서 기존에 비스테로이드성 항염증제(non-steroidal anti-inflammatory drug, NSAID) 및 해열제로 사용되고 있다. 그러나 두 화합물의 베타코로나바이러스(betacoronavirus)에 속하는 SARS-CoV-2 및 HCoV-OC43에 대한 항바이러스 효과는 알려진 바가 없다.On the other hand, rhein is an anthraquinone derivative and has an anti-inflammatory effect, so it has been used for the treatment of degenerative arthritis. It is used as a non-steroidal anti-inflammatory drug (NSAID) and as an antipyretic agent. However, the antiviral effect of the two compounds against SARS-CoV-2 and HCoV-OC43 belonging to betacoronaviruses is unknown.
본 발명자들은 베타코로나바이러스(Betacoronavirus)에 대한 항바이러스용 조성물을 개발하고자 예의 연구 노력하였다. 그 결과 레인(rhein), 메클로페남산(meclofenamic acid), 또는 이들의 조합을 유효성분으로 포함하는 조성물이 바이러스 RNA를 유의하게 억제하는 것을 규명함으로써, 본 발명을 완성하게 되었다.The present inventors made intensive research efforts to develop an antiviral composition for beta coronavirus . As a result, it was found that a composition comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient significantly inhibits viral RNA, thereby completing the present invention.
따라서, 본 발명의 목적은 레인(rhein), 메클로페남산(meclofenamic acid), 또는 이들의 조합을 유효성분으로 포함하는 베타코로나바이러스(Betacoronavirus)에 대한 항바이러스용 조성물을 제공하는 것이다. Accordingly, it is an object of the present invention to provide an antiviral composition for beta-coronavirus comprising rhein , meclofenamic acid, or a combination thereof as an active ingredient.
본 발명의 다른 목적은 레인(rhein), 메클로페남산(meclofenamic acid), 또는 이들의 조합을 유효성분으로 포함하는 SARS-CoV-2 및 HCoV-OC43에 대한 항바이러스용 조성물을 제공하는 것이다. Another object of the present invention is to provide an antiviral composition for SARS-CoV-2 and HCoV-OC43 comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient.
본 발명의 다른 목적은 COVID-19(Coronavirus Disease 2019)의 예방 또는 치료용 약제학적 조성물을 제공하는 것이다.Another object of the present invention is to provide a pharmaceutical composition for preventing or treating COVID-19 (Coronavirus Disease 2019).
본 발명의 또 다른 목적은 감기(common cold), 급성상기도염(acute upper respiratory tract infection), 중증 급성 호흡기 증후군(severe acute respiratory syndrome) 또는 바이러스성 폐렴(viral pneumonia)의 예방 또는 치료용 약제학적 조성물을 제공하는 것이다.Another object of the present invention is a pharmaceutical composition for the prevention or treatment of common cold, acute upper respiratory tract infection, severe acute respiratory syndrome or viral pneumonia is to provide
본 발명의 일 양태에 따르면, 본 발명은 레인(rhein), 메클로페남산(meclofenamic acid), 또는 이들의 조합을 유효성분으로 포함하는 베타코로나바이러스(Betacoronavirus)에 대한 항바이러스용 조성물을 제공한다.According to one aspect of the present invention, the present invention provides an antiviral composition for beta coronavirus comprising rhein , meclofenamic acid, or a combination thereof as an active ingredient. .
본 발명자들은 베타코로나바이러스(Betacoronavirus)에 대한 항바이러스용 조성물을 개발하고자 예의 연구 노력하였다. 그 결과 레인(rhein), 메클로페남산(meclofenamic acid), 또는 이들의 조합을 유효성분으로 포함하는 조성물이 바이러스 RNA를 유의하게 억제하는 것을 규명하였다.The present inventors made intensive research efforts to develop an antiviral composition for beta coronavirus . As a result, it was found that a composition comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient significantly inhibits viral RNA.
본 발명의 "레인(rhein)"이란 cassic acid 및 4,5-dihydroxy-9,10-dioxoanthracene-2-carboxylic acid로도 알려진 안트라퀴논(anthraquione) 유도체로서 항염증 효과를 가져 기존에 퇴행성관절염의 치료에 사용되고 있는, 다음의 화학식 1로 표기되는 화합물을 의미한다. "Rhein" of the present invention is an anthraquinone derivative, also known as cassic acid and 4,5-dihydroxy-9,10-dioxoanthracene-2-carboxylic acid, and has an anti-inflammatory effect. It refers to a compound represented by the following formula (1), which is being used.
[화학식 1][Formula 1]
본 발명의 "메클로페남산(meclofenamic acid)"이란 메클로페나미드산염(meclofenamate)으로도 알려진 안트라닐산(anthranilic acid) 유도체로서, COX(cyclooxygenase) 억제제이며 프로스타글란딘의 형성을 억제하는 효과를 가져 기존에 비스테로이드성 항염증제(non-steroidal anti-inflammatory drug, NSAID) 및 해열제로 사용되는, 다음의 화학식 2로 표기되는 화합물을 의미한다. The term "meclofenamic acid" of the present invention is an anthranilic acid derivative, also known as meclofenamate, a cyclooxygenase (COX) inhibitor, and has the effect of inhibiting the formation of prostaglandins. It refers to a compound represented by the following Chemical Formula 2, which is used as a non-steroidal anti-inflammatory drug (NSAID) and an antipyretic agent.
[화학식 2][Formula 2]
본 명세서의 용어 "유효성분으로 포함하는"이란, 레인(rhein), 메클로페남산(meclofenamic acid), 또는 이들의 조합의 약리학적 효능 또는 활성을 달성하는 데 충분한 양을 포함하는 것을 의미하고, 약물의 전달, 안정화 및 제제화를 위하여 다양한 성분이 부가적으로 첨가될 수 있는 것을 포함하는 의미이다.As used herein, the term "comprising as an active ingredient" means including an amount sufficient to achieve pharmacological efficacy or activity of rhein, meclofenamic acid, or a combination thereof, It means that various components may be additionally added for drug delivery, stabilization and formulation.
본 발명의 용어 "항바이러스용 조성물"이란 숙주 세포로의 바이러스 침입, 바이러스 유전체의 복제 및 합성, 바이러스 유전체의 전사, 바이러스의 단백질 합성, 역전사효소의 활성, 바이러스 조립(assembly) 또는 바이러스 출아(budding)를 억제함으로써, 바이러스의 감염을 예방하거나, 바이러스의 복제를 억제하거나, 바이러스의 전파를 방지하거나, 바이러스를 사멸하는 조성물 또는 바이러스 감염에 따라 발병하는 질병 또는 이에 의해 발현되는 증상을 치료하는 조성물을 의미한다. As used herein, the term "antiviral composition" refers to virus invasion into host cells, viral genome replication and synthesis, viral genome transcription, viral protein synthesis, reverse transcriptase activity, virus assembly or virus budding (budding). ) by inhibiting a composition for preventing infection of the virus, inhibiting the replication of the virus, preventing the spread of the virus, or killing the virus, or a composition for treating a disease caused by virus infection or symptoms expressed by it it means.
본 명세서의 용어 "예방"은 질환 또는 질환 상태의 방지 또는 보호적인 치료를 의미한다. 본 명세서의 용어 "치료"는 질환 상태의 감소, 억제, 진정, 또는 근절을 의미한다.As used herein, the term “prevention” refers to the prevention or protective treatment of a disease or disease state. As used herein, the term “treatment” means reducing, suppressing, sedating, or eradicating a disease state.
본 명세서에서 용어 '베타코로나바이러스(Betacoronavirus)'란 코로나바이러스 과(family Coronavirinae)에 속하는 네 개의 속(genus) 중 하나로서, 동물 및 인간에게 감염되어 무증상이거나 경증 내지 중증의 호흡기 증상을 유발하는 RNA 바이러스를 의미한다. As used herein, the term ' betacoronavirus ' is one of four genus belonging to the family Coronavirinae , and RNA that infects animals and humans and causes asymptomatic or mild to severe respiratory symptoms means virus.
본 발명의 일 구현예에 있어서, 본 발명의 베타코로나바이러스(Betacoronavirus)는 HCoV-OC43(human coronavirus OC43), HCoV-HKU1(human coronavirus HKU1), SARS-CoV(severe acute respiratory syndrome coronavirus), MERS-CoV(Middle East respiratory syndrome coronavirus) 및 SARS-CoV-2(severe acute respiratory syndrome coronavirus 2)를 포함한다.In one embodiment of the present invention, the beta coronavirus of the present invention is HCoV-OC43 (human coronavirus OC43 ), HCoV-HKU1 (human coronavirus HKU1), SARS-CoV (severe acute respiratory syndrome coronavirus), MERS- Middle East respiratory syndrome coronavirus (CoV) and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
본 발명의 일 구체예에 있어서, 본 발명의 베타코로나바이러스(Betacoronavirus)는 SARS-CoV-2(severe acute respiratory syndrome coronavirus 2) 및 HCoV-OC43(human coronavirus OC43)을 포함한다. In one embodiment of the present invention, beta coronavirus of the present invention includes SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) and HCoV-OC43 (human coronavirus OC43 ).
본 발명의 일 구현예에 있어서, 본 발명의 유효성분은 상기 베타코로나바이러스의 비구조단백질(non-structural protein, Nsp), 스파이크(spike, S), 피막(envelop, E), 막(membrane, M), 뉴클레오캡시드(nucleocapsid, N) 및 헤마글루티닌 에스터라제(haemagglutinin esterase, HE) 단백질로 이루어진 군으로부터 선택된 적어도 하나 이상의 바이러스 RNA의 수준을 억제하는 것을 특징으로 한다.In one embodiment of the present invention, the active ingredient of the present invention is the non-structural protein (Nsp), spike (S), envelope (E), membrane (membrane, M) of the beta coronavirus. ), nucleocapsid (nucleocapsid, N) and hemagglutinin esterase (haemagglutinin esterase, HE) characterized in that it inhibits the level of at least one viral RNA selected from the group consisting of proteins.
본 발명의 일 구체예에 있어서, 본 발명의 유효성분은 상기 베타코로나바이러스의 비구조단백질(non-structural protein, Nsp), 막(membrane, M) 단백질, 및 뉴클레오캡시드(nucleocapsid, N) 단백질로 이루어진 군으로부터 선택된 적어도 하나 이상의 바이러스 RNA의 수준을 억제하는 것을 특징으로 한다.In one embodiment of the present invention, the active ingredient of the present invention is a non-structural protein (Nsp), a membrane (M) protein, and a nucleocapsid (N) protein of the beta coronavirus. It is characterized in that it inhibits the level of at least one or more viral RNAs selected from the group consisting of.
본 발명의 용어 비구조단백질(non-structural protein, Nsp)이란 코로나바이러스의 복제 및 전사 관련 비구조단백질을 의미한다. 코로나바이러스의 비구조단백질에는 16개의 Nsp1 내지 Nsp16이 있고, Nsp3 및 Nsp5는 단백질분해 활성을 가지며, Nsp7, Nsp8 및 Nsp12는 복제효소-전사효소 복합체(replicase-transcriptase complex, RTC)를 형성한다. RTC의 핵심 구성요소인 Nsp12는 RNA-의존성 RNA 중합효소(RNA-dependent RNA polymerase, RdRp)이며 바이러스의 복제에서 RNA 합성을 직접적으로 매개한다.As used herein, the term non-structural protein (Nsp) refers to a non-structural protein related to the replication and transcription of coronavirus. Non-structural proteins of coronavirus include 16 Nsp1 to Nsp16, Nsp3 and Nsp5 have proteolytic activity, and Nsp7, Nsp8 and Nsp12 form a replicase-transcriptase complex (RTC). Nsp12, a key component of RTC, is an RNA-dependent RNA polymerase (RdRp) and directly mediates RNA synthesis in viral replication.
본 발명의 일 구체예에 있어서, 본 발명의 비구조단백질(non-structural protein, Nsp)은 Nsp1, Nsp2, Nsp3, Nsp4, Nsp5, Nsp6, Nsp7, Nsp8, Nsp9, Nsp10, Nsp11, Nsp12, Nsp13, Nsp14, Nsp15 및 Nsp16으로 이루어진 군으로부터 선택되는 1종 이상의 단백질이다. 본 발명의 다른 구체예에 있어서, 본 발명의 비구조단백질은 Nsp12이다.In one embodiment of the present invention, the non-structural protein (Nsp) of the present invention is Nsp1, Nsp2, Nsp3, Nsp4, Nsp5, Nsp6, Nsp7, Nsp8, Nsp9, Nsp10, Nsp11, Nsp12, Nsp13, Nsp14 , at least one protein selected from the group consisting of Nsp15 and Nsp16. In another embodiment of the present invention, the nonstructural protein of the present invention is Nsp12.
본 발명의 일 구현예에 있어서, 본 발명의 항바이러스용 조성물은 추가적으로 약제학적으로 허용 가능한 담체, 운반체, 부형제, 안정제 또는 희석제를 포함한다. In one embodiment of the present invention, the antiviral composition of the present invention additionally comprises a pharmaceutically acceptable carrier, carrier, excipient, stabilizer or diluent.
본 발명의 약제학적으로 허용 가능한 담체, 운반체, 부형제, 안정제 또는 희석제는 본 발명이 속하는 기술분야에서 통상적으로 사용되는 것으로 본 발명의 유효성분과 약리학적으로 양립 가능한 담체, 운반체, 부형제, 안정제, 또는 희석제를 의미한다. The pharmaceutically acceptable carrier, carrier, excipient, stabilizer or diluent of the present invention is commonly used in the art to which the present invention pertains and is pharmaceutically compatible with the active ingredient of the present invention. means
본 발명의 약제학적 조성물의 약제학적으로 허용 가능한 담체 또는 운반체에는 락토오스, 덱스트로오스, 수크로오스, 솔비톨, 만니톨, 전분, 아카시아 고무, 인산 칼슘, 알기네이트, 젤라틴, 규산 칼슘, 미세결정성 셀룰로스, 폴리비닐피롤리돈, 셀룰로스, 물, 시럽, 메틸 셀룰로스, 메틸히드록시벤조에이트, 프로필히드록시벤조에이트, 활석, 스테아르산 마그네슘, 미네랄 오일, 에탄올, DMSO(dimethyl sulfoxide) 등이 포함되나, 이에 한정되는 것은 아니다. 본 발명의 약제학적 조성물은 상기 성분들 이외에 부형제, 안정제, 희석제, 윤활제, 습윤제, 감미제, 향미제, 유화제, 현탁제, 보존제 등을 추가로 포함할 수 있다. 적합한 약제학적으로 허용 가능한 담체, 운반체, 부형제, 안정제 또는 희석제는 Remington's Pharmaceutical Sciences(19th ed., 1995)에 상세히 기재되어 있다. Pharmaceutically acceptable carriers or carriers of the pharmaceutical composition of the present invention include lactose, dextrose, sucrose, sorbitol, mannitol, starch, gum acacia, calcium phosphate, alginate, gelatin, calcium silicate, microcrystalline cellulose, poly vinylpyrrolidone, cellulose, water, syrup, methyl cellulose, methylhydroxybenzoate, propylhydroxybenzoate, talc, magnesium stearate, mineral oil, ethanol, dimethyl sulfoxide (DMSO), etc. it is not The pharmaceutical composition of the present invention may further include excipients, stabilizers, diluents, lubricants, wetting agents, sweeteners, flavoring agents, emulsifiers, suspending agents, preservatives, and the like, in addition to the above components. Suitable pharmaceutically acceptable carriers, carriers, excipients, stabilizers or diluents are described in detail in Remington's Pharmaceutical Sciences (19th ed., 1995).
본 발명의 약제학적 조성물은 경구 또는 비경구로 투여할 수 있고, 비경구 투여인 경우에는 정맥내 주입, 피하 주입, 근육 주입, 복강 주입, 경피 투여 등으로 투여할 수 있다.The pharmaceutical composition of the present invention may be administered orally or parenterally, and in the case of parenteral administration, it may be administered by intravenous injection, subcutaneous injection, intramuscular injection, intraperitoneal injection, transdermal administration, or the like.
본 발명의 약제학적 조성물의 적합한 투여량은 제제화 방법, 투여방식, 환자의 연령, 체중, 성, 병적 상태, 음식, 투여 시간, 투여 경로, 배설 속도 및 반응 감응성과 같은 요인들에 의해 다양하며, 보통으로 숙련된 의사는 소망하는 치료 또는 예방에 효과적인 투여량을 용이하게 결정 및 처방할 수 있다. 한편, 본 발명의 약제학적 조성물의 투여량은 바람직하게는 1일 당 0.0001-1000 mg/kg(체중)이다.A suitable dosage of the pharmaceutical composition of the present invention varies depending on factors such as formulation method, administration method, age, weight, sex, pathological condition, food, administration time, administration route, excretion rate and response sensitivity of the patient, An ordinarily skilled physician can readily determine and prescribe a dosage effective for the desired treatment or prophylaxis. Meanwhile, the dosage of the pharmaceutical composition of the present invention is preferably 0.0001-1000 mg/kg (body weight) per day.
본 발명의 약제학적 조성물은 당해 발명이 속하는 기술분야에서 통상의 지식을 가진 자가 용이하게 실시할 수 있는 방법에 따라, 약제학적으로 허용되는 담체 및/또는 부형제를 이용하여 제제화함으로써 단위 용량 형태로 제조되거나 또는 다용량 용기 내에 내입시켜 제조될 수 있다. 이때 제형은 오일 또는 수성 매질중의 용액, 현탁액 또는 유화액 형태이거나 엑스제, 분말제, 과립제, 정제 또는 캅셀제 형태일 수도 있으며, 분산제 또는 안정화제를 추가적으로 포함할 수 있다.The pharmaceutical composition of the present invention is prepared in unit dosage form by formulating using a pharmaceutically acceptable carrier and/or excipient according to a method that can be easily performed by a person of ordinary skill in the art to which the present invention pertains. or it may be prepared by incorporation into a multi-dose container. At this time, the formulation may be in the form of a solution, suspension, or emulsion in oil or aqueous medium, or may be in the form of an extract, powder, granule, tablet or capsule, and may additionally include a dispersant or stabilizer.
본 발명에서 사용된 포유동물 세포는 Vero 세포주(African green monkey kidney cell line), Calu-3 세포주(human lung adenocarcinoma cell line), HBEC 세포주(human bronchial epithelium cell line), 및 HCT-8 세포주(colon cancer cell line)로 이루어진 군으로부터 선택되는 적어도 하나 이상의 포유동물 세포를 포함하나, 이에 제한되는 것은 아니다. The mammalian cells used in the present invention include Vero cell line (African green monkey kidney cell line), Calu-3 cell line (human lung adenocarcinoma cell line), HBEC cell line (human bronchial epithelium cell line), and HCT-8 cell line (colon cancer). cell line), including at least one or more mammalian cells selected from the group consisting of, but not limited thereto.
본 발명의 Vero 세포주는 아프리카 녹색 원숭이(African green monkey)의 신장 상피 세포(kidney epithelial cell)로부터 분리된 세포주로서, 바이러스 배양의 숙주 세포로 흔히 사용된다. 본 발명의 Calu-3 세포주는 인간 폐암 세포로부터 유래된 세포주(human lung adenocarcinoma cell line)로서, 호흡기 감염 바이러스에 대한 연구에 흔히 사용되고 SARS-CoV-2 연구에서 사용된다. 본 발명의 HBEC 세포주는 인간 기관지 상피 세포주(human bronchial epithelium cell line)로서 세포 배양 연구에서 한 단계 더 나아가 실제 호흡기를 모방하도록 세포배양액-stem cell에서 분화된 bronchial epithelium cell-공기층으로 배양된 세포주이다. 본 발명의 HCT-8 세포는 대장암 세포주(colon cancer cell line)로서 HCoV-OC43 연구에 흔히 사용된 세포주이다.The Vero cell line of the present invention is a cell line isolated from kidney epithelial cells of an African green monkey, and is often used as a host cell for virus culture. The Calu-3 cell line of the present invention is a cell line derived from human lung cancer cells (human lung adenocarcinoma cell line), which is commonly used in research on respiratory infection viruses and is used in SARS-CoV-2 research. The HBEC cell line of the present invention is a human bronchial epithelium cell line, and a cell culture medium - bronchial epithelium cells differentiated from stem cells - is a cell line cultured in the air layer to mimic the actual respiratory system one step further in cell culture research. The HCT-8 cell of the present invention is a colon cancer cell line, a cell line commonly used in HCoV-OC43 research.
본 발명의 다른 일 양태에 따르면, 본 발명은 상술한 항바이러스용 조성물을 포함하는 COVID-19(coronavirus disease 2019)의 예방 또는 치료용 약제학적 조성물을 제공한다. 본 발명의 용어 "COVID-19"란 SARS-CoV-2 감염에 의한 호흡기 질환으로 코로나바이러스감염증-19(coronavirus disease 2019, COVID-19)를 의미하며, 무증상이거나 발열, 권태감, 기침, 호흡곤란, 폐렴, 가래, 인후통, 두통, 객혈, 오심, 설사 등을 포함하는 경증 내지 중증의 호흡기 증상을 나타낸다. COVID-19의 치료에는 현재 대증적인 치료로 수액 보충 및/또는 해열제의 사용 등의 보존적 치료가 있고 SARS-CoV-2에 대한 항바이러스제는 없는 실정이다.According to another aspect of the present invention, the present invention provides a pharmaceutical composition for preventing or treating COVID-19 (coronavirus disease 2019) comprising the above-described antiviral composition. As used herein, the term "COVID-19" is a respiratory disease caused by SARS-CoV-2 infection, meaning coronavirus disease 2019 (COVID-19), and is asymptomatic or has fever, malaise, cough, dyspnea, It shows mild to severe respiratory symptoms including pneumonia, sputum, sore throat, headache, hemoptysis, nausea, and diarrhea. Currently, as a symptomatic treatment for COVID-19, there are conservative treatments such as fluid supplementation and/or the use of antipyretic drugs, and there is no antiviral agent for SARS-CoV-2.
본 발명의 COVID-19(coronavirus disease 2019)의 예방 또는 치료용 약제학적 조성물은 상술한 본 발명의 다른 일 양태인 항바이러스용 조성물을 포함하므로, 본 명세서 기재의 과도한 복잡성을 피하기 위해 중복되는 내용을 원용하며, 그 기재를 생략한다. Since the pharmaceutical composition for the prevention or treatment of COVID-19 (coronavirus disease 2019) of the present invention includes the antiviral composition of another aspect of the present invention described above, overlapping contents are included in order to avoid excessive complexity of the present specification. cited, and the description thereof is omitted.
본 발명의 또 다른 양태에 따르면, 본 발명은 상술한 항바이러스용 조성물을 포함하는 감기(common cold), 급성상기도염(acute upper respiratory tract infection), 중증 급성 호흡기 증후군(severe acute respiratory syndrome) 또는 바이러스성 폐렴(viral pneumonia)의 예방 또는 치료용 약제학적 조성물을 제공한다. According to another aspect of the present invention, the present invention provides a common cold, acute upper respiratory tract infection, severe acute respiratory syndrome or virus comprising the above-described antiviral composition. It provides a pharmaceutical composition for preventing or treating viral pneumonia.
본 발명의 감기(common cold), 급성상기도염(acute upper respiratory tract infection), 중증 급성 호흡기 증후군(severe acute respiratory syndrome) 또는 바이러스성 폐렴(viral pneumonia)의 예방 또는 치료용 약제학적 조성물은 상술한 본 발명의 다른 일 양태인 항바이러스용 조성물을 포함하므로, 본 명세서 기재의 과도한 복잡성을 피하기 위해 중복되는 내용을 원용하며, 그 기재를 생략한다. The pharmaceutical composition for preventing or treating common cold, acute upper respiratory tract infection, severe acute respiratory syndrome, or viral pneumonia of the present invention is the present invention Since it includes the antiviral composition of another aspect of the present invention, overlapping content is cited in order to avoid excessive complexity of the description of the present specification, and the description thereof is omitted.
본 발명의 또 다른 일 양태에 따르면, 본 발명은 상술한 본 발명의 다른 일 양태에 따른 레인(rhein), 메클로페남산(meclofenamic acid), 또는 이들의 조합을 유효성분으로 포함하는 베타코로나바이러스(Betacoronavirus)에 대한 항바이러스용 조성물을 이를 필요로 하는 대상체에게 투여하는 단계를 포함하는 바이러스 억제 방법을 제공한다.According to another aspect of the present invention, the present invention is a beta coronavirus comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient according to another aspect of the present invention described above. (Betacoronavirus) provides a virus suppression method comprising administering an antiviral composition to a subject in need thereof.
본 발명의 또 다른 일 양태에 따르면, 본 발명은 상술한 본 발명의 다른 일 양태에 따른 레인(rhein), 메클로페남산(meclofenamic acid), 또는 이들의 조합을 유효성분으로 포함하는 베타코로나바이러스(Betacoronavirus)에 대한 항바이러스용 조성물을 이를 필요로 하는 대상체에게 투여하는 단계를 포함하는 바이러스 감염에 의한 질병 치료 방법을 제공한다.According to another aspect of the present invention, the present invention is a beta coronavirus comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient according to another aspect of the present invention described above. (Betacoronavirus) provides a method of treating a disease caused by a viral infection comprising administering an antiviral composition to a subject in need thereof.
본 발명의 바이러스 억제 방법 및 질병 치료 방법의 대상이 되는 바이러스와 질병은 상술한 항바이러스용 조성물에서 정의한 것과 같다.Viruses and diseases subject to the virus suppression method and disease treatment method of the present invention are the same as those defined in the antiviral composition described above.
본 발명의 일 구현예에 있어서, 본 발명의 대상체는 포유동물 또는 인간이다. 상기 포유동물은 개, 고양이, 소, 말, 돼지, 마우스, 랫트, 침팬지, 오랑우탄, 바분(baboon) 등을 포함하나, 이에 제한되는 것은 아니다.In one embodiment of the present invention, the subject of the present invention is a mammal or a human. The mammal includes, but is not limited to, dogs, cats, cows, horses, pigs, mice, rats, chimpanzees, orangutans, baboons, and the like.
본 발명의 상술한 바이러스 억제 방법 및 질병 치료 방법은 상술한 본 발명의 다른 일 양태에 따른 항바이러스용 조성물을 투여함으로써 이루어지므로, 중복되는 내용을 원용하며, 본 명세서 기재의 과도한 복잡성을 피하기 위해 그 기재를 생략한다.Since the above-described virus inhibition method and disease treatment method of the present invention are made by administering the antiviral composition according to another aspect of the present invention, overlapping contents are cited, and in order to avoid excessive complexity of the description of the present specification, the omit the description.
본 발명의 특징 및 이점을 요약하면 다음과 같다:The features and advantages of the present invention are summarized as follows:
(a) 본 발명은 레인(rhein), 메클로페남산(meclofenamic acid), 또는 이들의 조합을 유효성분으로 포함하는 베타코로나바이러스(Betacoronavirus)에 대한 항바이러스용 조성물을 제공한다. (a) The present invention provides an antiviral composition for beta coronavirus comprising rhein , meclofenamic acid, or a combination thereof as an active ingredient.
(b) 본 발명은 레인(rhein), 메클로페남산(meclofenamic acid), 또는 이들의 조합을 유효성분으로 포함하는 SARS-CoV-2 및 HCoV-OC43에 대한 항바이러스용 조성물을 제공한다.(b) The present invention provides an antiviral composition for SARS-CoV-2 and HCoV-OC43 comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient.
(c) 본 발명은 레인(rhein), 메클로페남산(meclofenamic acid), 또는 이들의 조합을 유효성분으로 포함하는 베타코로나바이러스(Betacoronavirus)에 대한 항바이러스용 조성물을 이를 필요로 하는 대상체에게 투여하는 단계를 포함하는 바이러스 억제 방법을 제공한다.(c) the present invention is administered to a subject in need of an antiviral composition for beta coronavirus comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient It provides a virus suppression method comprising the step of.
(d) 본 발명은 레인(rhein), 메클로페남산(meclofenamic acid), 또는 이들의 조합을 유효성분으로 포함하는 베타코로나바이러스(Betacoronavirus)에 대한 항바이러스용 조성물을 이를 필요로 하는 대상체에게 투여하는 단계를 포함하는 바이러스 감염에 의한 질병 치료 방법을 제공한다.(d) the present invention is administered to a subject in need of a composition for antiviral against beta-coronavirus comprising rhein, meclofenamic acid, or a combination thereof as an active ingredient It provides a method for treating diseases caused by viral infection comprising the step of:
(e) 본 발명의 항바이러스용 조성물을 이용하는 경우, 베타코로나바이러스의 RNA 수준을 억제함으로써 COVID-19(coronavirus disease 2019), 감기(common cold), 급성상기도염(acute upper respiratory tract infection), 중증 급성 호흡기 증후군(severe acute respiratory syndrome) 또는 바이러스성 폐렴(viral pneumonia)을 예방하거나 치료할 수 있다. (e) when using the antiviral composition of the present invention, by suppressing the RNA level of beta-coronavirus, COVID-19 (coronavirus disease 2019), common cold, acute upper respiratory tract infection (acute upper respiratory tract infection), severe It can prevent or treat severe acute respiratory syndrome or viral pneumonia.
도 1a 내지 1d는 SARS-CoV-2 또는 HCoV-OC43에 감염된 세포에 레인(rhein)을 포함하는 항바이러스용 조성물의 처리 여부에 따른 qRT-PCR로 측정한 바이러스 RNA 수준(level)을 나타낸다. 도 1a는 SARS-CoV-2에 감염된 Calu-3 세포(SARS-CoV-2-infected Calu-3), 도 1b는 SARS-CoV-2에 감염된 Vero 세포(SARS-CoV-2-infected Vero), 도 1c는 HCoV-OC43에 감염된 HCT-8 세포(HCoV OC43-infected HCT-8) 및 도 1d는 HCoV-OC43에 감염된 Vero 세포(HCoV OC43-infected Vero)에서 바이러스 RNA 수준을 나타낸다. 모든 RNA 수준은 각각의 GAPDH의 RNA 수준으로 보정되었다. 1A to 1D show the viral RNA levels measured by qRT-PCR according to whether or not SARS-CoV-2 or HCoV-OC43-infected cells are treated with an antiviral composition including rhein. Figure 1a shows Calu-3 cells infected with SARS-CoV-2 (SARS-CoV-2-infected Calu-3), Figure 1b shows Vero cells infected with SARS-CoV-2 (SARS-CoV-2-infected Vero); 1C shows viral RNA levels in HCoV-OC43 infected HCT-8 cells (HCoV OC43-infected HCT-8) and FIG. 1D shows viral RNA levels in HCoV-OC43 infected Vero cells (HCoV OC43-infected Vero). All RNA levels were corrected for the RNA level of each GAPDH.
도 2a 내지 2e는 SARS-CoV-2 또는 HCoV-OC43에 감염된 세포에 메클로페남산(meclofenamic acid, MA)을 포함하는 항바이러스용 조성물의 처리 여부에 따른 qRT-PCR로 측정한 바이러스 RNA 수준을 나타낸다. 도 2a는 SARS-CoV-2에 감염된 Calu-3 세포(SARS-CoV-2-infected Calu-3), 도 2b는 SARS-CoV-2에 감염된 HBEC 세포(SARS-CoV-2-infected HBEC), 도 2c는 SARS-CoV-2에 감염된 Vero 세포(SARS-CoV-2-infected Vero), 도 2d는 HCoV-OC43에 감염된 HCT-8 세포(HCoV OC43-infected HCT-8) 및 도 2e는 HCoV-OC43에 감염된 Vero 세포(HCoV OC43-infected Vero)에서 바이러스 RNA 수준을 나타낸다. 모든 RNA 수준은 각각의 GAPDH의 RNA 수준으로 보정되었다. 2a to 2e show the viral RNA levels measured by qRT-PCR according to whether or not the SARS-CoV-2 or HCoV-OC43-infected cells were treated with an antiviral composition containing meclofenamic acid (MA). indicates. Figure 2a shows Calu-3 cells infected with SARS-CoV-2 (SARS-CoV-2-infected Calu-3), Figure 2b shows HBEC cells infected with SARS-CoV-2 (SARS-CoV-2-infected HBEC); Fig. 2c shows Vero cells infected with SARS-CoV-2 (SARS-CoV-2-infected Vero), Fig. 2d shows HCT-8 cells infected with HCoV-OC43 (HCoV OC43-infected HCT-8), and Fig. 2e shows HCoV- Viral RNA levels in OC43-infected Vero cells (HCoV OC43-infected Vero) are shown. All RNA levels were corrected for the RNA level of each GAPDH.
이하, 실시예를 통하여 본 발명을 더욱 상세히 설명하고자 한다. 이들 실시예는 오로지 본 발명을 보다 구체적으로 설명하기 위한 것으로, 본 발명의 요지에 따라 본 발명의 범위가 이들 실시예에 의해 제한되지 않는다는 것은 당업계에서 통상의 지식을 가진 자에 있어서 자명할 것이다.Hereinafter, the present invention will be described in more detail through examples. These examples are only for illustrating the present invention in more detail, and it will be apparent to those of ordinary skill in the art that the scope of the present invention is not limited by these examples according to the gist of the present invention. .
실시예Example
실시예 1: 항바이러스용 조성물의 제조Example 1: Preparation of antiviral composition
실시예 1-1: 레인(Rhein)을 포함하는 항바이러스용 조성물의 제조Example 1-1: Preparation of antiviral composition comprising Rhein
레인(Rhein)은 Sigma-Aldrich(카탈로그 번호 R7269)에서 구매하여 운반체 DMSO에서 5 μM, 10 μM, 25 μM 및 50 μM 농도의 레인(rhein)을 포함하는 항바이러스용 조성물을 제조하였고, 대조군으로서 DMSO만을 포함하는 조성물 또는 50%(v/v) DMSO 및 50%(v/v) 에탄올의 혼합용액(DMSO + Ethanol)을 제조하였다.Rhein was purchased from Sigma-Aldrich (Catalog No. R7269) to prepare an antiviral composition comprising rhein at concentrations of 5 μM, 10 μM, 25 μM and 50 μM in vehicle DMSO, DMSO as a control. A composition containing only or a mixed solution of 50% (v/v) DMSO and 50% (v/v) ethanol (DMSO + Ethanol) was prepared.
실시예 1-2: 메클로페남산(Meclofenamic acid, MA)을 포함하는 항바이러스용 조성물의 제조Example 1-2: Preparation of antiviral composition containing meclofenamic acid (MA)
메클로페남산(Meclofenamic acid, MA)은 Sigma-Aldrich(카탈로그 번호 M4531)에서 구매하여 운반체 에탄올에서 0.5 μM, 5 μM, 10 μM, 25 μM, 50 μM 및 100 μM 농도의 메클로페남산(MA)을 포함하는 항바이러스용 조성물을 제조하였고, 대조군으로서 에탄올만을 포함하는 조성물 또는 50%(v/v) DMSO 및 50%(v/v) 에탄올의 혼합용액(DMSO + Ethanol)을 제조하였다.Meclofenamic acid (MA) was purchased from Sigma-Aldrich (Cat. No. M4531) and prepared in carrier ethanol at concentrations of 0.5 µM, 5 µM, 10 µM, 25 µM, 50 µM and 100 µM meclofenamic acid (MA). ) was prepared, and as a control, a composition containing only ethanol or a mixed solution of 50% (v/v) DMSO and 50% (v/v) ethanol (DMSO + Ethanol) was prepared.
실시예 2: 세포주Example 2: Cell Lines
실시예 2-1: Vero 세포주Example 2-1: Vero cell line
Vero 세포주(African green monkey kidney cell line, ATCC(American Type Culture Collection), 카탈로그 번호: CCL-81)는 10% FBS(fetal bovine serum)가 첨가된 DMEM(Dulbecco's Modified Eagle Medium)으로 37℃ 및 5% CO2의 배양기에서 배양하였다.Vero cell line (African green monkey kidney cell line, ATCC (American Type Culture Collection), catalog number: CCL-81) was treated with DMEM (Dulbecco's Modified Eagle Medium) supplemented with 10% FBS (fetal bovine serum) at 37°C and 5% It was cultured in an incubator of CO 2 .
실시예 2-2: Calu-3 세포주Example 2-2: Calu-3 cell line
Calu-3 세포주(human lung adenocarcinoma cell line, 한국세포주은행(Korean Cell Line Bank, KCLB), KCLB 번호: 30055)는 10% FBS가 첨가된 DMEM으로 37℃ 및 5% CO2의 배양기에서 배양하였다.Calu-3 cell line (human lung adenocarcinoma cell line, Korean Cell Line Bank (KCLB), KCLB No.: 30055) was cultured in DMEM with 10% FBS added at 37° C. and 5% CO 2 in an incubator.
실시예 2-3: HCT-8 세포주Example 2-3: HCT-8 cell line
HCT-8 세포주(colon cancer cell line, 한국세포주은행, KCLB 번호: 10244)는 10% FBS가 첨가된 RPMI(Rosewell Park Memorial Institute) 배양액으로 37℃ 및 5% CO2의 배양기에서 배양하였다.The HCT-8 cell line (colon cancer cell line, Korea Cell Line Bank, KCLB No.: 10244) was cultured in an RPMI (Rosewell Park Memorial Institute) culture medium supplemented with 10% FBS at 37° C. and 5% CO 2 in an incubator.
실시예 2-4: HBEC 세포주Example 2-4: HBEC cell line
HBEC 세포주(human bronchial epithelium cell line, ATCC, 카탈로그 번호: PCS-300-010)는 STEMCELLTM Technologies에서 제공하는 프로토콜을 필요한 부분만 약간 수정하여(mutatis mutandis) 배양하였다. The HBEC cell line (human bronchial epithelium cell line, ATCC, catalog number: PCS-300-010) was cultured by slightly modifying the protocol provided by STEMCELL TM Technologies ( mutatis mutandis ).
보다 상세하게, HBEC 세포의 배양 시작일부터 3일째까지는 i) 배양액 PneumaCultTM-Ex plus medium(STEMCELLTM Technologies, 카탈로그 #05040)에 0.1 μg/ml의 하이드로코르티손(hydrocortisone, Sigma, 카탈로그 #H0888)을 첨가한 배양액에서 배양하였다. More specifically, from the start of the culture of HBEC cells to the 3rd day i) 0.1 μg/ml of hydrocortisone (hydrocortisone, Sigma, catalog #H0888) was added to the culture medium PneumaCult TM -Ex plus medium (STEMCELL TM Technologies, catalog #05040). It was cultured in one culture medium.
HBEC 세포의 분화를 위해, 배양 후 4일째부터 45일째까지는 ii) 상기 3일 동안 배양한 HBEC 세포를 3Х105 세포/웰 씩 12-웰 플레이트(아래의 Basal Chamber와 위의 Apical Chamber 사이에 0.4 μm-pore 막(membrane)을 갖는 Transwell® insert, STEMCELLTM Technologies, 카탈로그 #05001)의 Apical Chamber에서 0.5 ml의 배양액 PneumaCultTM-Ex plus medium(STEMCELLTM Technologies)으로 배양하였다. 상기 12-웰 플레이트의 Basal Chamber에는 웰 당 1 ml의 배양액(PneumaCultTM-Ex plus medium, STEMCELLTM Technologies)을 첨가하였다. HBEC 세포를 배양하였던 상기 12-웰 플레이트의 Apical Chamber에서 세포 집합도(cell confluency)가 100%에 도달하면, Apical Chamber에서 배양액을 제거하여 분화(differentiation)를 유도하였다. 상기 분화 배양을 통해 HBEC 세포는 생체 내 인간의 기도(airway) 상피와 형태학적 및 기능적으로 유사한 거짓중층상피(pseudostratified epithelium)를 형성하였다. For differentiation of HBEC cells, from the 4th day to the 45th day after culture ii) HBEC cells cultured for the above 3 days were placed in a 12-well plate (0.4 μm between the Basal Chamber below and the Apical Chamber above) at 3Х10 5 cells/well. Transwell® insert with -pore membrane, STEMCELL TM Technologies, catalog #05001) in the Apical Chamber of 0.5 ml of the culture medium PneumaCult TM -Ex plus medium (STEMCELL TM Technologies) was cultured. 1 ml of culture solution (PneumaCult TM -Ex plus medium, STEMCELL TM Technologies) was added per well to the Basal Chamber of the 12-well plate. When the cell confluency reached 100% in the apical chamber of the 12-well plate in which the HBEC cells were cultured, the culture medium was removed from the apical chamber to induce differentiation. Through the differentiation culture, HBEC cells formed a pseudostratified epithelium that is morphologically and functionally similar to human airway epithelium in vivo.
상기 분화 배양을 시작하고 30일까지는 12-웰 플레이트의 Basal Chamber에서 배양액 PneumaCultTM-ALI maintenance medium(STEMCELLTM Technologies, 카탈로그 #05002, 05003 및 05006, 1 μg/ml의 하이드로코르티손을 첨가함)으로 2일에 1회씩 배양액을 교체하였다. 이 후 7일 동안은 상기 배양액으로 1주 2회씩 배양액을 교체하였고, 또 다음의 7일 동안은 1주 1회씩 배양액을 교체하였다.From the start of the differentiation culture to 30 days, the culture medium PneumaCult TM -ALI maintenance medium (STEMCELL TM Technologies, catalog #05002, 05003 and 05006, 1 μg/ml of hydrocortisone is added) in a 12-well plate Basal Chamber 2 The culture medium was changed once a day. After that, the culture medium was replaced with the culture medium twice a week for 7 days, and the culture medium was changed once a week for the next 7 days.
배양 후 45일째에는 iii) 상기 분화되어 유지된 HBEC 세포에 베타코로나바이러스를 감염시켰으며, iV) 배양 후 47일째, 즉 바이러스 감염 후 48시간에 RNA 추출을 위해 샘플을 얻었다.On day 45 after culture, iii) the differentiated and maintained HBEC cells were infected with beta-coronavirus, and iV) samples were obtained for RNA extraction on day 47 after culture, that is, 48 hours after virus infection.
실시예 3: 바이러스Example 3: Virus
실시예 3-1: SARS-CoV-2Example 3-1: SARS-CoV-2
SARS-CoV-2(severe acute respiratory syndrome coronavirus 2)는 질병관리본부 산하 국가병원체자원은행에서 분양받은 병원체자원이며, 국제백신연구소의 생물안전 3등급(biosafety level 3) 연구 시설에서 엄격한 통제하에 관리되었다.SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) is a pathogen resource purchased from the National Pathogen Resource Bank under the Korea Centers for Disease Control and Prevention, and was managed under strict control at the International Vaccine Research Institute's biosafety level 3 research facility. .
실시예 3-2: HCoV-OC43Example 3-2: HCoV-OC43
HCoV OC43(human coronavirus OC43)은 고려대학교 병원성바이러스은행에서 분양받았으며 생물안전 2등급 연구 시설에서 관리하였다. HCoV OC43 (human coronavirus OC43) was purchased from the Pathogenic Virus Bank of Korea University and managed at a biosafety level 2 research facility.
실시예 4: 베타코로나바이러스의 감염 및 항바이러스용 조성물의 처리Example 4: Infection of beta-coronavirus and treatment of antiviral composition
실시예 4-1: SARS-CoV-2 또는 HCoV-OC43에 감염된 세포주에서 레인(Rhein)을 포함하는 항바이러스용 조성물의 처리Example 4-1: Treatment of an antiviral composition comprising Rhein in a cell line infected with SARS-CoV-2 or HCoV-OC43
1) SARS-CoV-2에 감염된 Calu-3 세포(SARS-CoV-2-infected Calu-3)1) SARS-CoV-2 infected Calu-3 cells (SARS-CoV-2-infected Calu-3)
Calu-3 세포주를 12-웰 플레이트(12-well plate)에 1.75Х105 세포/웰 씩 세 개의 웰(well)에 배양하였다. 배양 18시간 후에 무-혈청(serum-free) DMEM으로 각 웰을 세척하여 생물안전 3등급 연구 시설에서 SARS-CoV-2를 각 웰에 0.05의 MOI(multiplicity of infection)로 감염시켰으며, 2% FBS를 포함하는 DMEM에서 배양하였다. 바이러스 감염과 동시에 25 μM 농도의 레인(Rhein)을 포함하는 항바이러스용 조성물과 대조군으로서 DMSO를 각 웰의 세포배양액에 처리하였다. 바이러스 감염 후 24시간에 RNA 추출을 위한 샘플을 얻었다. The Calu-3 cell line was cultured in three wells of 1.75Х10 5 cells/well in a 12-well plate. After 18 hours of incubation, each well was washed with serum-free DMEM and each well was infected with SARS-CoV-2 at a multiplicity of infection (MOI) of 0.05 in a biosafety grade 3 research facility, 2% Cultured in DMEM containing FBS. Simultaneously with virus infection, an antiviral composition containing 25 μM concentration of Rhein and DMSO as a control were treated in the cell culture medium of each well. Samples for RNA extraction were obtained 24 hours after viral infection.
2) SARS-CoV-2에 감염된 Vero 세포(SARS-CoV-2-infected Vero)2) Vero cells infected with SARS-CoV-2 (SARS-CoV-2-infected Vero)
Vero 세포주를 12-웰 플레이트에 1.75Х105 세포/웰 씩 세 개의 웰에 배양하였다. 배양 18시간 후 무-혈청 DMEM으로 각 웰을 세척하여 생물안전 3등급 연구 시설에서 SARS-CoV-2를 0.05의 MOI로 감염시켰고, 2% FBS를 포함하는 DMEM에서 배양하였다. 바이러스 감염과 동시에 25 μM 농도의 레인(Rhein)을 포함하는 항바이러스용 조성물과 대조군으로서 DMSO를 각 웰(well)의 세포배양액에 처리하였다. 바이러스 감염 후 24시간에 RNA 추출을 위한 샘플을 얻었다.The Vero cell line was cultured in three wells of 1.75Х10 5 cells/well in a 12-well plate. After 18 hours of incubation, each well was washed with serum-free DMEM and infected with SARS-CoV-2 at an MOI of 0.05 in a biosafety grade 3 research facility, and cultured in DMEM containing 2% FBS. Simultaneously with virus infection, an antiviral composition containing 25 μM concentration of Rhein and DMSO as a control were treated in the cell culture medium of each well. Samples for RNA extraction were obtained 24 hours after viral infection.
3) HCoV-OC43에 감염된 HTC-8 세포(HCoV-OC43-infected HCT-8)3) HTC-8 cells infected with HCoV-OC43 (HCoV-OC43-infected HCT-8)
HCT-8 세포주를 12-웰 플레이트에 2Х105 세포/웰 씩 두 개의 웰에 배양하였다. 배양 후 18시간에 PBS 또는 3% FBS를 포함하는 RPMI로 각 웰을 세척한 후 생물안전 2등급 연구 시설에서 HCoV-OC43를 감염시켰고, 3% FBS를 포함하는 RPMI에서 배양하였다. 바이러스 감염과 동시에 0.25 μM, 2.5 μM, 25 μM 및 250 μM 농도의 레인(Rhein)을 포함하는 항바이러스용 조성물과 대조군으로서 DMSO 및 에탄올의 혼합용액을 각 웰의 세포배양액에 처리하였다. 바이러스 감염 후 24시간에 각 웰을 PBS 또는 3% FBS를 포함하는 RPMI로 세척한 후 RNA 추출을 위한 샘플을 얻었다.The HCT-8 cell line was cultured in two wells of 2Х10 5 cells/well in a 12-well plate. After washing each well with RPMI containing PBS or 3% FBS 18 hours after incubation, HCoV-OC43 was infected in a biosafety grade 2 research facility, and cultured in RPMI containing 3% FBS. Simultaneously with virus infection, a mixed solution of DMSO and ethanol as a control and an antiviral composition containing Rhein at 0.25 μM, 2.5 μM, 25 μM and 250 μM concentrations was treated in the cell culture medium of each well. 24 hours after virus infection, each well was washed with PBS or RPMI containing 3% FBS to obtain a sample for RNA extraction.
4) HCoV-OC43에 감염된 Vero 세포(HCoV-OC43-infected Vero)4) HCoV-OC43-infected Vero cells (HCoV-OC43-infected Vero)
Vero 세포주를 12-웰 플레이트에 2Х105 세포/웰 씩 세 개의 웰에 배양하였다. 배양 18시간 후 PBS 또는 3% FBS를 포함하는 DMEM으로 각 웰을 세척한 후 생물안전 2등급 연구 시설에서 HCoV-OC43를 감염시켰고, 3% FBS를 포함하는 DMEM에서 배양하였다. 바이러스 감염과 동시에 5 μM, 10 μM, 25 μM 및 50 μM 농도의 레인(Rhein)을 포함하는 항바이러스용 조성물과 대조군으로서 DMSO를 각 웰(well)의 세포배양액에 처리하였다. 바이러스 감염 후 24시간에 PBS 또는 3% FBS를 포함하는 DMEM으로 세척한 후 RNA 추출을 위한 샘플을 얻었다.The Vero cell line was cultured in three wells of 2Х10 5 cells/well in a 12-well plate. After 18 hours of incubation, each well was washed with DMEM containing PBS or 3% FBS, and then infected with HCoV-OC43 in a biosafety grade 2 research facility, and cultured in DMEM containing 3% FBS. Simultaneously with virus infection, an antiviral composition containing 5 μM, 10 μM, 25 μM and 50 μM concentration of Rhein and DMSO as a control were treated in the cell culture medium of each well. 24 hours after virus infection, samples for RNA extraction were obtained after washing with PBS or DMEM containing 3% FBS.
실시예 4-2: SARS-CoV-2 또는 HCoV-OC43가 감염된 세포주에서 메클로페남산(meclofenamic acid, MA)을 포함하는 항바이러스용 조성물의 처리Example 4-2: Treatment of an antiviral composition containing meclofenamic acid (MA) in a cell line infected with SARS-CoV-2 or HCoV-OC43
처리한 항바이러스용 조성물의 종류와 SARS-CoV-2에 감염된 HBEC 세포를 제외하고는 상기 실시예 4-1에 기재된 조건과 동일 내지 유사한 조건으로 각 세포주를 배양하여 각 바이러스를 감염시켰으므로, 본 명세서 기재의 과도한 복잡성을 피하기 위해 중복되는 내용을 원용하며, 그 기재를 생략한다.Since each cell line was cultured under the same or similar conditions as those described in Example 4-1, except for the type of the treated antiviral composition and the HBEC cells infected with SARS-CoV-2, each virus was infected. In order to avoid excessive complexity of the description of the specification, overlapping content is cited and description thereof is omitted.
SARS-CoV-2에 감염된 Calu-3 세포(SARS-CoV-2-infected Calu-3), SARS-CoV-2에 감염된 HBEC 세포(SARS-CoV-2-infected HBEC) 및 SARS-CoV-2에 감염된 Vero 세포(SARS-CoV-2-infected Vero)에 50 μM 농도의 메클로페남산(Meclofenamic acid, MA)을 포함하는 항바이러스용 조성물과 대조군으로서 에탄올을 각 웰의 세포배양액에 처리하였다.SARS-CoV-2-infected Calu-3 cells (SARS-CoV-2-infected Calu-3), SARS-CoV-2 infected HBEC cells (SARS-CoV-2-infected HBEC) and SARS-CoV-2 Infected Vero cells (SARS-CoV-2-infected Vero) were treated with an antiviral composition containing 50 μM concentration of meclofenamic acid (MA) and ethanol as a control to the cell culture medium of each well.
또한, HCoV-OC43에 감염된 HTC-8 세포(HCoV-OC43-infected HCT-8)에는 0.5 μM, 5 μM 및 50 μM 농도의 메클로페남산(Meclofenamic acid, MA)을 포함하는 항바이러스용 조성물과 대조군으로서 DMSO 및 에탄올의 혼합용액(DMSO + Ethanol)을 각 웰의 세포배양액에 처리하였고, HCoV-OC43에 감염된 Vero 세포(HCoV-OC43-infected Vero)에는 5 μM, 10 μM, 25 μM, 50 μM 및 100 μM 농도의 메클로페남산(Meclofenamic acid, MA)을 포함하는 항바이러스용 조성물과 대조군으로서 DMSO을 각 웰의 세포배양액에 처리하였다.In addition, in HCoV-OC43-infected HTC-8 cells (HCoV-OC43-infected HCT-8), an antiviral composition containing 0.5 μM, 5 μM and 50 μM of meclofenamic acid (MA) and As a control, a mixed solution of DMSO and ethanol (DMSO + Ethanol) was treated in each well of the cell culture medium, and 5 μM, 10 μM, 25 μM, 50 μM for HCoV-OC43-infected Vero cells (HCoV-OC43-infected Vero). And an antiviral composition containing 100 μM of meclofenamic acid (MA) and DMSO as a control were treated in the cell culture medium of each well.
1) SARS-CoV-2에 감염된 HBEC 세포(SARS-CoV-2-infected HBEC)1) SARS-CoV-2 infected HBEC cells (SARS-CoV-2-infected HBEC)
실시예 2-4와 같이, 배양한 HBEC 세포주를 배양 후 3일째에 분화시키며 유지하였고, 배양 후 45일째에 생물안전 3등급 연구 시설에서 PBS로 각 웰을 세척한 후 SARS-CoV-2를 3.3Х104 pfu(plaque-forming unit)로 감염시켰다. 상기 바이러스 감염 2시간 전에 50 μM 농도의 메클로페남산(Meclofenamic acid, MA)을 포함하는 항바이러스용 조성물과 대조군으로서 에탄올을 각 웰의 세포배양액에 처리하였다. 배양 후 47일째, 즉 바이러스 감염 후 48시간 뒤에 PBS로 각 웰을 세척한 후 RNA 추출을 위한 샘플을 얻었다.As in Example 2-4, the cultured HBEC cell line was differentiated and maintained on the 3rd day after culturing, and on the 45th day after culturing, each well was washed with PBS in a biosafety grade 3 research facility, and then SARS-CoV-2 was 3.3 Infected with Х10 4 pfu (plaque-forming unit). Two hours before the virus infection, an antiviral composition containing 50 μM of meclofenamic acid (MA) and ethanol as a control were treated in the cell culture medium of each well. At 47 days after culture, that is, 48 hours after virus infection, each well was washed with PBS, and then samples for RNA extraction were obtained.
실시예 5: RNA 분리 및 정제Example 5: RNA Isolation and Purification
상기 실시예 4에서 얻은 RNA 추출을 위한 샘플에 핵산추출용해액 Trizol(Invitrogen, 카탈로그 번호 10296028)을 처리하여 전체 RNA를 분리하였다. SARS-CoV-2에 감염된 세포의 전체 RNA는 PureLinkTM RNA Mini Kit(Invitrogen, 카탈로그 번호: 12183018A)를, HCoV-OC43에 감염된 세포의 전체 RNA는 RNeasy Mini Kit(Qiagen, 카탈로그 번호: 74106)를 이용하여 제조사의 프로토콜을 따라 정제하였다. 정제된 RNA의 농도는 분광광도계(NanoDropTM 2000c Spectrophotometer, ND-2000C, Thermo Scientific)를 이용하여 측정하였다.The sample for RNA extraction obtained in Example 4 was treated with a nucleic acid extraction solution Trizol (Invitrogen, catalog number 10296028) to isolate total RNA. Total RNA from cells infected with SARS-CoV-2 was obtained using the PureLink TM RNA Mini Kit (Invitrogen, catalog number: 12183018A), and total RNA from cells infected with HCoV-OC43 was obtained using the RNeasy Mini Kit (Qiagen, catalog number: 74106). and purified according to the manufacturer's protocol. The concentration of purified RNA was measured using a spectrophotometer (NanoDrop TM 2000c Spectrophotometer, ND-2000C, Thermo Scientific).
실시예 6: qRT-PCR(quantative real-time PCR)Example 6: quantitative real-time PCR (qRT-PCR)
상기 실시예 5에서 얻은 정제된 RNA는 Power SYBRTM Green PCR Master Mix(Applied BiosystemsTM, 카탈로그 번호: 4367659)와 실시간 유전자 증폭 장비(Real-time QuantStudio 3 Real-Time PCR Instrument, Applied BiosystemsTM)로 qRT-PCR를 수행하였다. The purified RNA obtained in Example 5 was qRT with Power SYBR TM Green PCR Master Mix (Applied Biosystems TM , catalog number: 4367659) and real-time gene amplification equipment (Real-time QuantStudio 3 Real-Time PCR Instrument, Applied Biosystems TM ). -PCR was performed.
qRT-PCR 실험에 사용된 프라이머(primer)의 정방향(forward, F) 및 역방향 (reverse, R)의 서열은 다음의 표 1에 제시하였다. SARS-CoV-2에 감염된 세포에서 NSP12(non-structural protein 12), M(membrane) 및 N(nucleocapsid)의 바이러스 RNA 수준을 측정하는 경우, 서열번호 1 내지 6에 나타낸 올리고뉴클레오타이드 서열을 가지는 프라이머를 사용하였다. SARS-CoV-2에 감염된 Calu-3 및 HBEC 세포에서 GAPDH의 RNA를 측정하는 경우, 서열번호 7 및 8에 나타낸 올리고뉴클레오타이드 서열을 가지는 프라이머를 사용하였다. SARS-CoV-2에 감염된 Vero 및 HCT-8 세포에서 GAPDH의 RNA를 측정하는 경우, 서열번호 9 및 10에 나타낸 올리고뉴클레오타이드 서열을 가지는 프라이머를 사용하였다. HCoV-OC43에 감염된 세포에서 N(nucleocapsid)의 바이러스 RNA 수준의 측정을 위해 서열번호 11 및 12에 나타낸 올리고뉴클레오타이드 서열을 가지는 프라이머를 사용하였다. The sequences of the forward (forward, F) and reverse (reverse, R) of the primers used in the qRT-PCR experiment are presented in Table 1 below. When measuring viral RNA levels of NSP12 (non-structural protein 12), M (membrane) and N (nucleocapsid) in SARS-CoV-2 infected cells, primers having the oligonucleotide sequences shown in SEQ ID NOs: 1 to 6 were used. was used. When measuring RNA of GAPDH in Calu-3 and HBEC cells infected with SARS-CoV-2, primers having the oligonucleotide sequences shown in SEQ ID NOs: 7 and 8 were used. When measuring RNA of GAPDH in Vero and HCT-8 cells infected with SARS-CoV-2, primers having the oligonucleotide sequences shown in SEQ ID NOs: 9 and 10 were used. For the measurement of the viral RNA level of N (nucleocapsid) in HCoV-OC43-infected cells, primers having the oligonucleotide sequences shown in SEQ ID NOs: 11 and 12 were used.
| 유전자명gene name | F/RF/R | 서열order | 서열번호SEQ ID NO: |
| NSP12NSP12 | FF | CAG AGA GCT AGG TGT TGT ACCAG AGA GCT AGG TGT TGT AC | 1One |
| NSP12NSP12 | RR | AAG CAC GTA GTG CGT TTA TCAAG CAC GTA GTG CGT TTA TC | 22 |
| MM | FF | CGT GCC ACT CCA TGG CAC TATCGT GCC ACT CCA TGG CAC TAT | 33 |
| MM | RR | CGT CCT AGA TGG TGT CCA GCA ACGT CCT AGA TGG TGT CCA GCA A | 44 |
| NN | FF | GGC CAG AAG CTG GAC TTC CCGGC CAG AAG CTG GAC TTC CC | 55 |
| NN | RR | AGG ATT GCG GGT GCC AAT GTAGG ATT GCG GGT GCC AAT GT | 66 |
| GAPDHGAPDH | FF | CTC TCT GCT CCT CCT GTT CGA CCTC TCT GCT CCT CCT GTT CGA C | 77 |
| GAPDHGAPDH | RR |
TGA GCG ATG TGG CTC GGC TTGA GCG ATG TGG |
88 |
| GAPDHGAPDH | FF | TGC CAA CGT GTC AGT GGT GTGC CAA CGT GTC AGT GGT G | 99 |
| GAPDHGAPDH | RR | GCC TGC TTC ACC ACC TTC TTGGCC TGC TTC ACC ACC TTC TTG | 1010 |
| NN | FF | TAA GCA ATC CAG TAG TAG AGC GTAA GCA ATC CAG TAG TAG AGC G | 1111 |
| NN | RR | TCT AAA CTG GTC GGA CTG ATTCT AAA CTG GTC GGA CTG AT | 1212 |
qRT-PCR 실험 결과로 얻은 nsp12(non-structural protein 12), 막(membrane, M) 단백질 및 뉴클레오캡시드(nucleocapsid, N) 단백질 유전자의 Ct(Cycle threshold) 값을 내인성 대조군인 GAPDH의 Ct값으로 보정하여(normalized) 2-ΔΔCt의 방법을 이용해 바이러스 RNA 수준을 분석하였다.The Ct (Cycle threshold) values of nsp12 (non-structural protein 12), membrane (M) protein and nucleocapsid (N) protein genes obtained as a result of qRT-PCR experiments were used as Ct values of GAPDH, an endogenous control. Virus RNA levels were analyzed using the method of 2 -ΔΔCt with normalized.
본 발명의 실험은 2회 반복을 수행한 HCoV-OC43에 감염된 HCT-8 세포 실험을 제외하고는 모두 적어도 세 번 반복되었고, 도 1a 내지 1d 및 도 2a 내지 2e의 그래프상의 오차 선(error bar)은 표준오차(standard error of the mean)를 나타낸다.The experiment of the present invention was repeated at least three times except for the HCT-8 cell infection infected with HCoV-OC43, which was repeated twice, and the error bar on the graph of FIGS. 1A to 1D and 2A to 2E is the standard error of the mean.
실시예 7: 레인(Rhein)을 포함하는 항바이러스용 조성물의 베타코로나바이러스 RNA의 억제 효과Example 7: Inhibitory effect of beta-coronavirus RNA of antiviral composition comprising Rhein
실시예 7-1: SARS-CoV-2에 대한 레인(Rhein)을 포함하는 항바이러스용 조성물의 바이러스 RNA 억제 효과Example 7-1: Virus RNA inhibitory effect of antiviral composition containing Rhein on SARS-CoV-2
SARS-CoV-2를 감염시킨 Calu-3 세포 및 Vero 세포에 DMSO만을 처리한 대조군과 25 μM의 레인(Rhein)을 포함하는 항바이러스용 조성물을 처리한 실험군에서 qRT-PCR로 측정한 nsp12, M 및 N의 바이러스 RNA 수준을 GAPDH로 보정하여 분석하였다(도 1a 및 도 1b 참조). SARS-CoV-2를 감염시킨 Calu-3 세포(SARS-CoV-2-infected Calu-3)에서 DMSO만을 처리한 대조군에 비해 25 μM의 레인(Rhein)을 포함하는 항바이러스용 조성물을 처리한 실험군에서 nps12, M, 및 N의 바이러스 RNA 수준이 모두 5% 미만으로 유의하게 억제되었고(도 1a 참조), SARS-CoV-2를 감염시킨 Vero 세포(SARS-CoV-2-infected Vero)에서 또한 레인(Rhein)을 포함하는 항바이러스용 조성물을 처리한 실험군에서 nps12, M, 및 N의 바이러스 RNA 수준이 모두 약 30% 미만(도 1b 참조)으로 유의하게 억제되었다.nsp12, M measured by qRT-PCR in the control group treated with SARS-CoV-2-infected Calu-3 cells and Vero cells only with DMSO and the experimental group treated with the antiviral composition containing 25 μM lane (Rhein) And virus RNA levels of N were analyzed by correcting them with GAPDH (see FIGS. 1A and 1B ). In Calu-3 cells infected with SARS-CoV-2 (SARS-CoV-2-infected Calu-3), compared to the control group treated only with DMSO, the experimental group treated with an antiviral composition containing 25 μM of Rhein The viral RNA levels of nps12, M, and N were all significantly suppressed by less than 5% (see Fig. 1a), and in Vero cells infected with SARS-CoV-2 (SARS-CoV-2-infected Vero) also lane In the experimental group treated with the antiviral composition containing (Rhein), the viral RNA levels of nps12, M, and N were all significantly inhibited to less than about 30% (see FIG. 1b ).
실시예 7-2: HCoV-OC43에 대한 레인(Rhein)을 포함하는 항바이러스용 조성물의 바이러스 RNA 억제 효과 Example 7-2: Virus RNA inhibitory effect of antiviral composition containing Rhein on HCoV-OC43
HCoV-OC43를 감염시킨 HCT-8 세포(HCoV OC43-infected HCT-8)에 DMSO와 에탄올의 혼합액(DMSO+Ethanol)을 처리한 대조군과 0.25 μM, 2.5 μM, 25 μM 및 250 μM의 레인(Rhein)을 포함하는 항바이러스용 조성물을 처리한 실험군에서(도 1c 참조), HCoV-OC43를 감염시킨 Vero 세포(HCoV OC43-infected Vero)에 DMSO만을 처리한 대조군과 5 μM, 10 μM, 25 μM 및 50 μM의 레인(Rhein)을 포함하는 항바이러스용 조성물을 처리한 실험군에서(도 1d 참조) qRT-PCR로 측정한 각각 N의 바이러스 RNA 수준을 GAPDH로 보정하여 분석하였다. HCoV-OC43-infected HCT-8 cells (HCoV OC43-infected HCT-8) were treated with a mixture of DMSO and ethanol (DMSO+Ethanol) in the control group and lanes (Rhein) of 0.25 μM, 2.5 μM, 25 μM and 250 μM ) in the experimental group treated with an antiviral composition containing In the experimental group treated with the antiviral composition containing 50 μM of Rhein (see FIG. 1d ), the viral RNA level of each N measured by qRT-PCR was analyzed by correcting it with GAPDH.
HCoV-OC43를 감염시킨 HCT-8 세포에 250 μM 및 25 μM의 레인(Rhein)을 포함하는 항바이러스용 조성물을 처리한 경우와 HCoV-OC43를 감염시킨 Vero 세포에 5 μM, 10 μM, 25 μM 및 50 μM의 레인(Rhein)을 포함하는 항바이러스용 조성물을 처리한 경우에 N의 바이러스 RNA 수준이 유의하게 억제되었다. 또한, 도 1d에 나타낸 바와 같이, HCoV-OC43를 감염시킨 Vero 세포에서 처리한 항바이러스용 조성물 내 레인(Rhein)의 농도가 증가함에 따라 N의 RNA 수준의 억제가 증가하는 용량-의존적 효과(dose-dependent effect)를 확인하였다.When HCT-8 cells infected with HCoV-OC43 were treated with an antiviral composition containing 250 μM and 25 μM of Rhein, and Vero cells infected with HCoV-OC43 were treated with 5 μM, 10 μM, 25 μM And when the antiviral composition comprising 50 μM of lane (Rhein) was treated, the viral RNA level of N was significantly suppressed. In addition, as shown in FIG. 1d , as the concentration of Rhein in the antiviral composition treated in Vero cells infected with HCoV-OC43 increased, the inhibition of the RNA level of N increased - a dose-dependent effect (dose -dependent effect) was confirmed.
실시예 8: 메클로페남산(Meclofenamic acid, MA)을 포함하는 항바이러스용 조성물의 바이러스 RNA의 억제 효과Example 8: Inhibitory effect of antiviral composition containing meclofenamic acid (MA) on viral RNA
실시예 8-1: SARS-CoV-2에 대한 메클로페남산(Meclofenamic acid, MA)을 포함하는 항바이러스용 조성물의 바이러스 RNA 억제 효과Example 8-1: Virus RNA inhibitory effect of antiviral composition containing meclofenamic acid (MA) on SARS-CoV-2
SARS-CoV-2를 감염시킨 Calu-3 세포(SARS-CoV-2-infected Calu-3), HBEC 세포(SARS-CoV-2-infected HBEC) 및 Vero 세포(SARS-CoV-2-infected Vero)에 에탄올만을 처리한 대조군과 50 μM의 메클로페남산(Meclofenamic acid, MA)을 포함하는 항바이러스용 조성물을 처리한 실험군에서 qRT-PCR로 측정한 nsp12, M 및 N의 바이러스 RNA 수준을 GAPDH로 보정하여 분석하였다(도 2a, 도 2b 및 도 2c 참조). SARS-CoV-2를 감염시킨 Calu-3 세포와 Vero 세포(SARS-CoV-2-infected Vero)에서는 에탄올만을 처리한 대조군에 비해 50 μM의 MA를 포함하는 항바이러스용 조성물을 처리한 실험군에서 nps12, M 및 N의 바이러스 RNA 수준이 모두 5% 미만으로 유의하게 억제되었고(도 2a 및 도 2c 참조), SARS-CoV-2를 감염시킨 HBEC 세포(SARS-CoV-2-infected HBEC)의 경우에는 약 40% 이하로 유의하게 억제되었다(도 2b 참조).Calu-3 cells infected with SARS-CoV-2 (SARS-CoV-2-infected Calu-3), HBEC cells (SARS-CoV-2-infected HBEC) and Vero cells (SARS-CoV-2-infected Vero) In the control group treated with only ethanol and the experimental group treated with the antiviral composition containing 50 μM meclofenamic acid (MA), the viral RNA levels of nsp12, M and N measured by qRT-PCR were measured with GAPDH. The analysis was corrected (refer to FIGS. 2A, 2B and 2C). In Calu-3 cells and Vero cells infected with SARS-CoV-2 (SARS-CoV-2-infected Vero), nps12 in the experimental group treated with the antiviral composition containing 50 μM MA compared to the control group treated only with ethanol. , M and N were all significantly suppressed by less than 5% (see FIGS. 2a and 2c ), and in the case of SARS-CoV-2-infected HBEC cells (SARS-CoV-2-infected HBEC), It was significantly suppressed by about 40% or less (see Fig. 2b).
실시예 8-2: HCoV-OC43에 대한 메클로페남산(Meclofenamic acid, MA)을 포함하는 항바이러스용 조성물의 바이러스 RNA 억제 효과Example 8-2: Virus RNA inhibitory effect of antiviral composition containing meclofenamic acid (MA) on HCoV-OC43
HCoV-OC43를 감염시킨 HCT-8 세포(HCoV OC43-infected HCT-8)에 DMSO와 에탄올을 처리한 대조군과 0.5 μM, 5 μM 및 50 μM의 메클로페남산(Meclofenamic acid, MA)을 포함하는 항바이러스용 조성물을 처리한 실험군에서(도 2d 참조), HCoV-OC43를 감염시킨 Vero 세포(HCoV OC43-infected Vero)에 DMSO만을 처리한 대조군과 5 μM, 10 μM, 25 μM, 50 μM 및 100 μM의 MA를 포함하는 항바이러스용 조성물을 처리한 실험군에서(도 2e 참조) qRT-PCR로 측정한 N의 바이러스 RNA 수준을 GAPDH로 보정하여 분석하였다. HCoV-OC43를 감염시킨 HCT-8 세포에 50 μM의 MA를 포함하는 항바이러스용 조성물을 처리한 경우와 HCoV-OC43를 감염시킨 Vero 세포에 10 μM, 25 μM, 50 μM 및 100 μM의 MA를 포함하는 항바이러스용 조성물을 처리한 경우에 N의 바이러스 RNA 수준이 유의하게 억제되었음을 확인하였다.A control group treated with DMSO and ethanol in HCoV-OC43-infected HCT-8 cells (HCoV OC43-infected HCT-8) and 0.5 μM, 5 μM and 50 μM of meclofenamic acid (Meclofenamic acid, MA) containing In the experimental group treated with the antiviral composition (see Fig. 2d), Vero cells infected with HCoV-OC43 (HCoV OC43-infected Vero) were treated only with DMSO and 5 μM, 10 μM, 25 μM, 50 μM and 100 In the experimental group treated with the antiviral composition containing μM MA (see Fig. 2e), the viral RNA level of N measured by qRT-PCR was analyzed by correcting it with GAPDH. When HCT-8 cells infected with HCoV-OC43 were treated with an antiviral composition containing 50 μM MA, and Vero cells infected with HCoV-OC43 were treated with 10 μM, 25 μM, 50 μM and 100 μM of MA. It was confirmed that the viral RNA level of N was significantly suppressed when the composition for antiviral containing was treated.
Claims (7)
- 레인(rhein), 메클로페남산(meclofenamic acid), 또는 이들의 조합을 유효성분으로 포함하는 베타코로나바이러스(Betacoronavirus)에 대한 항바이러스용 조성물.Rain (rhein), meclofenamic acid (meclofenamic acid), or beta coronavirus comprising a combination thereof as an active ingredient ( Betacoronavirus ) Antiviral composition for.
- 제 1 항에 있어서, 상기 베타코로나바이러스(Betacoronavirus)는 HCoV-OC43(human coronavirus OC43), HCoV-HKU1(human coronavirus HKU1), SARS-CoV(severe acute respiratory syndrome coronavirus), MERS-CoV(Middle East respiratory syndrome coronavirus) 및 SARS-CoV 2(severe acute respiratory syndrome coronavirus 2)를 포함하는 것인, 항바이러스용 조성물.According to claim 1, wherein the beta coronavirus ( Betacoronavirus ) is HCoV-OC43 (human coronavirus OC43), HCoV-HKU1 (human coronavirus HKU1), SARS-CoV (severe acute respiratory syndrome coronavirus), MERS-CoV (Middle East respiratory) Syndrome coronavirus) and SARS-CoV 2 (severe acute respiratory syndrome coronavirus 2), which includes, an antiviral composition.
- 제 1 항에 있어서, 상기 유효성분은 상기 베타코로나바이러스의 비구조단백질(non-structural protein, Nsp), 스파이크(spike, S), 피막(envelop, E), 막(membrane, M), 뉴클레오캡시드(nucleocapsid, N) 및 헤마글루티닌 에스터라제(haemagglutinin esterase, HE) 단백질로 이루어진 군으로부터 선택된 적어도 하나 이상의 바이러스 RNA 수준을 억제하는 것을 특징으로 하는, 항바이러스용 조성물.The method according to claim 1, wherein the active ingredient is a non-structural protein (Nsp), spike (S), envelope (E), membrane (M), nucleocapsid of the beta coronavirus. (nucleocapsid, N) and hemagglutinin esterase (haemagglutinin esterase, HE) characterized in that it inhibits the level of at least one virus RNA selected from the group consisting of proteins, antiviral composition.
- 제 3 항에 있어서, 상기 비구조단백질(non-structural protein, Nsp)은 Nsp1, Nsp2, Nsp3, Nsp4, Nsp5, Nsp6, Nsp7, Nsp8, Nsp9, Nsp10, Nsp11, Nsp12, Nsp13, Nsp14, Nsp15 및 Nsp16으로 이루어진 군으로부터 선택되는 1종 이상의 단백질인 것인, 항바이러스용 조성물.According to claim 3, wherein the non-structural protein (non-structural protein, Nsp) is Nsp1, Nsp2, Nsp3, Nsp4, Nsp5, Nsp6, Nsp7, Nsp8, Nsp9, Nsp10, Nsp11, Nsp12, Nsp13, Nsp14, Nsp15 and Nsp16. One or more proteins selected from the group consisting of, antiviral composition.
- 제 1 항에 있어서, 상기 항바이러스용 조성물은 추가적으로 약제학적으로 허용 가능한 담체, 운반체, 부형제, 안정제 또는 희석제를 포함하는 항바이러스용 조성물.The antiviral composition of claim 1, wherein the antiviral composition additionally comprises a pharmaceutically acceptable carrier, carrier, excipient, stabilizer or diluent.
- 제 1 항 내지 제 5 항 중 어느 한 항의 항바이러스용 조성물을 포함하는 COVID-19(coronavirus disease 2019)의 예방 또는 치료용 약제학적 조성물.A pharmaceutical composition for preventing or treating COVID-19 (coronavirus disease 2019) comprising the antiviral composition of any one of claims 1 to 5.
- 제 1 항 내지 제 5 항 중 어느 한 항의 항바이러스용 조성물을 포함하는 감기(common cold), 급성상기도염(acute upper respiratory tract infection), 중증 급성 호흡기 증후군(severe acute respiratory syndrome) 또는 바이러스성 폐렴(viral pneumonia)의 예방 또는 치료용 약제학적 조성물.A common cold, acute upper respiratory tract infection, severe acute respiratory syndrome, or viral pneumonia comprising the antiviral composition of any one of claims 1 to 5 ( A pharmaceutical composition for preventing or treating viral pneumonia).
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US18/037,386 US20240009159A1 (en) | 2020-11-17 | 2021-02-01 | Antiviral composition for sars-cov-2 and hcov-oc43 comprising rhein, meclofenamic acid, or a combination thereof |
| EP21894778.6A EP4248961A1 (en) | 2020-11-17 | 2021-02-01 | Antiviral composition for sars-cov-2 and hcov-oc43 comprising rhein, meclofenamic acid, or a combination thereof |
| JP2023530069A JP2023550409A (en) | 2020-11-17 | 2021-02-01 | Antiviral composition against SARS-CoV-2 and HCoV-OC43 comprising rhein, meclofenamic acid, or a combination thereof |
| CN202180077470.6A CN117042760A (en) | 2020-11-17 | 2021-02-01 | Antiviral composition against SARS-CoV-2 and HCoV-OC43 comprising rhein, meclofenamic acid or a combination thereof |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR10-2020-0154110 | 2020-11-17 | ||
| KR1020200154110A KR20220067429A (en) | 2020-11-17 | 2020-11-17 | Antiviral composition against SARS-CoV-2 and HCoV-OC43 comprising rhein, meclofenamic acid, or combination thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2022107999A1 true WO2022107999A1 (en) | 2022-05-27 |
Family
ID=81709266
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/KR2021/001312 WO2022107999A1 (en) | 2020-11-17 | 2021-02-01 | Antiviral composition for sars-cov-2 and hcov-oc43 comprising rhein, meclofenamic acid, or a combination thereof |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20240009159A1 (en) |
| EP (1) | EP4248961A1 (en) |
| JP (1) | JP2023550409A (en) |
| KR (1) | KR20220067429A (en) |
| CN (1) | CN117042760A (en) |
| WO (1) | WO2022107999A1 (en) |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111265508A (en) * | 2018-12-05 | 2020-06-12 | 中检科医药科技(北京)集团有限公司 | Use of diacerein in preparing antiviral medicine and treating virus infection |
| CN111346075A (en) * | 2020-03-24 | 2020-06-30 | 深圳市金汇球高科技有限公司 | Application of rhubarb anthraquinone extract in broad-spectrum antiviral |
| US20200237689A1 (en) * | 2018-11-15 | 2020-07-30 | Bluewillow Biologics, Inc. | Prevention and treatment of coronavirus and other respiratory infections using nanoemulsion compositions |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101857685B1 (en) | 2017-09-22 | 2018-05-14 | 주식회사 코젠바이오텍 | Primers and probes for simultaneous detection of subtypes of coronavirus and detecting method for coronavirus using the same |
-
2020
- 2020-11-17 KR KR1020200154110A patent/KR20220067429A/en not_active Application Discontinuation
-
2021
- 2021-02-01 WO PCT/KR2021/001312 patent/WO2022107999A1/en active Application Filing
- 2021-02-01 EP EP21894778.6A patent/EP4248961A1/en not_active Withdrawn
- 2021-02-01 US US18/037,386 patent/US20240009159A1/en active Pending
- 2021-02-01 CN CN202180077470.6A patent/CN117042760A/en not_active Withdrawn
- 2021-02-01 JP JP2023530069A patent/JP2023550409A/en not_active Abandoned
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20200237689A1 (en) * | 2018-11-15 | 2020-07-30 | Bluewillow Biologics, Inc. | Prevention and treatment of coronavirus and other respiratory infections using nanoemulsion compositions |
| CN111265508A (en) * | 2018-12-05 | 2020-06-12 | 中检科医药科技(北京)集团有限公司 | Use of diacerein in preparing antiviral medicine and treating virus infection |
| CN111346075A (en) * | 2020-03-24 | 2020-06-30 | 深圳市金汇球高科技有限公司 | Application of rhubarb anthraquinone extract in broad-spectrum antiviral |
Non-Patent Citations (5)
| Title |
|---|
| "Remington's Pharmaceutical Sciences", 1995 |
| ADNAN SHAH: "Novel Coronavirus-Induced NLRP3 Inflammasome Activation: A Potential Drug Target in the Treatment of COVID-19", FRONTIERS IN IMMUNOLOGY, vol. 11, 19 May 2020 (2020-05-19), pages 1021, XP055724935, DOI: 10.3389/fimmu.2020.01021 * |
| CHANDEL VAISHALI, RAJ SIBI, RATHI BRIJESH, KUMAR DHRUV: "In Silico Identification of Potent COVID-19 Main Protease Inhibitors from FDA Approved Antiviral Compounds and Active Phytochemicals through Molecular Docking: A Drug Repurposing Approach", 20 March 2020 (2020-03-20), pages 1 - 28, XP055931398, [retrieved on 20220614], DOI: 10.20944/preprints202003.0349.v1 * |
| PAREEK, R. P.: "Use of Mefenamic Acid as a Supportive Treatment of COVID-19: A Repurposing Drug. ", INTERNATIONAL JOURNAL OF SCIENCE AND RESEARCH(IJSR)., vol. 9, no. 6, 1 June 2020 (2020-06-01), pages 69 - 73, XP055931402, DOI: 10.21275/SR20530150407 * |
| SEOUL NATIONAL UNIVERSITY R & DB FOUNDATION: "Support for Research and Operation expenses of the Institute of Basic Science", 3 March 2020, NATIONAL RESEARCH FOUNDATION, article "International Science Business Belt Construction" |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20220067429A (en) | 2022-05-24 |
| CN117042760A (en) | 2023-11-10 |
| US20240009159A1 (en) | 2024-01-11 |
| JP2023550409A (en) | 2023-12-01 |
| EP4248961A1 (en) | 2023-09-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN111557939B (en) | Use of favipiravir for the treatment of coronavirus infections | |
| US20080075695A1 (en) | Combination therapy method for treating hepatitis c virus infection and pharmaceutical compositions for use therein | |
| WO2021040337A1 (en) | Niclosamide delayed-release composition and antiviral use thereof | |
| WO2009148279A9 (en) | Triterpenoid-based compound used as a virus inhibitor | |
| CN113521289A (en) | Application of 15 effective components of medicine in resisting virus infection | |
| WO2022107999A1 (en) | Antiviral composition for sars-cov-2 and hcov-oc43 comprising rhein, meclofenamic acid, or a combination thereof | |
| WO2021194290A1 (en) | Pharmaceutical composition for preventing or treating epidemic rna viral infectious disease | |
| EP4116296A1 (en) | Anti-rna virus drug and application thereof | |
| WO2022173165A1 (en) | Composition containing black ginseng as active ingredient for prevention, alleviation, or treatment of coronavirus infection | |
| WO2021215798A1 (en) | Pharmaceutical composition for treating sars-coronavirus infection, and medical use thereof | |
| WO2022045520A1 (en) | Composition for treating coronavirus-19 infection, comprising phenanthroindolizidine and phenanthroquinolizidine alkaloid derivative, optical isomer thereof, or pharmaceutically acceptable salt thereof as active ingredient | |
| WO2019212203A1 (en) | Composition for preventing or inhibiting influenza virus infection, containing ginseng berry polysaccharides | |
| CN113440527A (en) | Application of naphthoquine or naphthoquine-containing combined preparation in resisting coronavirus | |
| WO2023182840A1 (en) | Antiviral pharmaceutical composition and use thereof | |
| WO2022146070A1 (en) | Anti-coronavirus pharmaceutical composition containing hepatitis b virus-derived polypeptide | |
| WO2022014813A1 (en) | Pharmaceutical composition for preventing or treating sars-cov-2 infection | |
| WO2022216053A1 (en) | Anti-coronavirus co-administration therapeutic composition comprising coronavirus cell entry inhibitor and coronavirus protease activity inhibitor | |
| EP4108241A1 (en) | Anti-rna virus drug and application thereof | |
| WO2023090947A1 (en) | Pharmaceutical composition for preventing or treating coronavirus infectious disease | |
| WO2022154542A1 (en) | Prophylactic administration method against respiratory virus, comprising administering interferon-beta to potential respiratory virus-infected subject | |
| WO2021235695A1 (en) | Preventive or therapeutic pharmaceutical composition for coronavirus infection comprising tetraarsenic hexoxide | |
| CN113197894B (en) | Application of olbatik in preparation of broad-spectrum anti-coronavirus medicines | |
| WO2021210852A1 (en) | Anti-viral composition comprising placenta-derived material | |
| WO2021215616A1 (en) | Composition for treating coronavirus infection or infectious disease, comprising polyphosphates | |
| US20220204501A1 (en) | Enterovirus inhibitor |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 21894778 Country of ref document: EP Kind code of ref document: A1 |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 202180077470.6 Country of ref document: CN Ref document number: 18037386 Country of ref document: US Ref document number: 2023530069 Country of ref document: JP |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| ENP | Entry into the national phase |
Ref document number: 2021894778 Country of ref document: EP Effective date: 20230619 |